About: A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis

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About: A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 1993

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rdf:type	Item
description	wetenschappelijk artikel (nl) bài báo khoa học (vi) наукова стаття, опублікована в січні 1993 (uk) im Jahr 1993 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 1993 (ast) artikull shkencor i botuar më 01 janar 1993 (sq) scientific article published on 01 January 1993 (en) գիտական հոդված հրատարակված 1993 թվականի հունվարի 1-ին (hy)
publication date	wds:Q70659381-60A999D1-EEC9-410E-8419-62DBE8D4251B
publication date	1993-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q70659381-02CB3594-57CF-4930-AA1B-BBE5320DC7DA wds:Q70659381-0DB1B1E8-C272-4AF0-8C3A-D4B2E0B37B08 wds:Q70659381-4865147B-0914-46D7-9FA3-1EAE6F6A0894 wds:Q70659381-59AC23A6-31DC-472D-84D0-FFE5CFA4100E wds:Q70659381-6DCBC434-A2D1-4FC1-AB5E-D6BF44B4DE64 wds:Q70659381-7021B91B-E83F-416B-9435-C6F7E8ECB9CA wds:Q70659381-72D95213-A11E-4BC5-BC59-08029636B6C1 wds:Q70659381-7C00D536-50B2-41B0-AAAA-C49AB165F8A2 wds:Q70659381-8F04C0FE-691B-4D85-A125-FC4CFD955DFB wds:Q70659381-96DC6B22-50DA-4F85-8502-63DE3428442D wds:Q70659381-A443AA65-D5B0-4492-A517-E752E2F70F98 wds:Q70659381-AFB760CF-515A-4A9B-8D16-2BB0E69A43C4 wds:Q70659381-B33828EB-CEE4-4C9F-B9CA-E9AB721063AA wds:Q70659381-B89B1401-FB8E-408B-8DCB-3F333FCD32E5 wds:Q70659381-B9222659-B677-4B82-9905-84ECEAD431E1 wds:Q70659381-BF1A3BB9-C53B-4F9B-A5C9-570960C67ED9 wds:Q70659381-C2758ED1-7468-4F45-BECD-15AFDFDFEA74 wds:Q70659381-CC318520-33BD-4850-A3FF-B7EA4458F5F2 wds:Q70659381-E1A492D9-FD29-4EA6-877C-3375DD611E8B wds:Q70659381-E4F1FAB9-5F14-46CF-B4BF-52A81573E363 wds:Q70659381-E513436A-5AC2-4356-8A7A-BE5400A63E38 wds:Q70659381-E576550A-76AE-409C-AB21-D3F492AE2CA5 wds:Q70659381-F8307D31-75C7-4351-8507-C43A7D1AF123
cites work	Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy. Genetic aspects of antibiotic induced deafness: mitochondrial inheritance Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation Two-locus mitochondrial and nuclear gene models for mitochondrial disorders Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation A new look at the statistical model identification Sensorineural deafness inherited as a tissue specific mitochondrial disorder Maternal inheritance of human mitochondrial DNA Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA. X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation Regressive logistic models for familial disease and other binary traits On the statistical determination of major gene mechanisms in continuous human traits: regressive models. Relaxed Cellular Controls and Organelle Heredity Complete replacement of mitochondrial DNA in Drosophila Biochemical characterization of a pedigree with mitochondrially inherited deafness Variable genotype of Leber's hereditary optic neuropathy patients. A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy The generation of transplasmic Drosophila simulans by cytoplasmic injection: effects of segregation and selection on the perpetuation of mitochondrial DNA heteroplasmy. Probability functions on complex pedigrees Segregation analysis in human genetics Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy On some models for segregation analysist?
author name string	wds:Q70659381-25C6A618-C76C-4C59-A27A-B45636709C6B wds:Q70659381-59E0AEAE-AFF6-4B10-817C-E001C13258F8 wds:Q70659381-D751B54C-EEA8-47D9-A99D-0BE03E363EF5
author name string	Jaber L Shohat M Bu X
rdfs:label	A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (en) A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (nl) A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (sq)
skos:prefLabel	A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (en) A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (nl) A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (sq)
name	A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (en) A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (nl) A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (sq)
author	wds:Q70659381-CBF52F87-3A2F-4E13-A457-4DB16EA3C04D
author	Jerome I Rotter
title	wds:Q70659381-EFDE30EE-986B-42EA-A7F7-2B53E1EFDB3A
title	A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis (en)
page(s)	wds:Q70659381-A5456653-CBF5-4711-863E-81D7BC8B0D9C
page(s)	3-15
instance of	wds:Q70659381-24921CB1-F231-41D3-8AC6-5328F728B096
instance of	scholarly article
main subject	wds:Q70659381-A394823B-EFE1-4018-8B00-0B432387894A
main subject	deafness
PubMed ID	wds:Q70659381-004744D4-9CAA-4C2E-97F2-BA46F213649A
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8472932
PubMed ID	8472932
published in	wds:Q70659381-4FCEBB54-F87D-47AE-A91B-768A229EEE95
published in	Genetic Epidemiology
issue	wds:Q70659381-C4C04467-B48C-4C0F-ACB6-403497C06B90
volume	wds:Q70659381-D2A48E89-8252-43E8-A547-3D52C5C91F5F
issue	1
volume	10
DOI	wds:Q70659381-3AA8FCBE-448D-485C-B1A7-A42FBF550359
DOI	http://dx.doi.org/10.1002/GEPI.1370100102
DOI	10.1002/GEPI.1370100102
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70659381
is cites work of	Candidate locus for a nuclear modifier gene for maternally inherited deafness Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness. Genetics of hearing loss: where are we standing now? An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds

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