About: Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation

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About: Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation Goto Sponge NotDistinct Permalink

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scientific article published on January 2008

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) bài báo khoa học (vi) article scientifique (fr) artículu científicu espublizáu en 2008 (ast) наукова стаття, опублікована в січні 2008 (uk) scientific article published on January 2008 (en) مقالة علمية نشرت في يناير 2008 (ar)
publication date	wds:Q37184910-8807FADE-7832-403C-9CD2-313112108D58
publication date	2008-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q37184910-00BA0F58-B245-4C98-A8D9-AE8209CB15E8 wds:Q37184910-3D2B748C-35F2-43A3-95E9-EB050EE96EDD wds:Q37184910-461CD13F-1E74-4E06-AE7B-22CB67AEBCFA wds:Q37184910-4E1F0277-4B0F-49E2-9139-78230B2AC01B wds:Q37184910-5344D0F6-AD23-4819-A7FF-085FCB4447A4 wds:Q37184910-5AE95A88-1A60-4ACC-B96A-BF98131A5842 wds:Q37184910-7FE7AB52-A25D-4F19-B341-A973A6EF1D2F wds:Q37184910-A5E776A8-0EE3-46E9-ACEA-62B147B5EEB3 wds:Q37184910-FEE9D5C2-0389-458F-98B3-DE82AC0275C6
author name string	Patrick J Willems Imre Gerlinger Béla Melegh Katalin Komlósi György Kosztolányi Kinga Hadzsiev Zsolt Szabó Károly Méhes Anita Maász
rdfs:label	Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (en) Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (nl) Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (ast)
skos:prefLabel	Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (en) Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (nl) Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (ast)
name	Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (en) Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (nl) Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (ast)
title	wds:Q37184910-140167DD-D4BB-493E-84DB-37C719AD52BD
title	Phenotypic variants of the deafness-associated mitochondrial DNA A7445G mutation (en)
page(s)	wds:Q37184910-9C03DB7B-D657-4DD2-867E-2D60DBF60EC6
page(s)	1257-1262
instance of	wds:Q37184910-377100D3-E1F2-40AA-903F-215BC030BA5F wds:Q37184910-dee3a09e-b415-4583-9dce-21014b54d3fb
instance of	review article scholarly article
main subject	wds:Q37184910-4478EAB9-1A58-47FD-862B-D42CA3245015 wds:Q37184910-64428C0A-676C-4DFE-AAA3-2E931D764C51 wds:Q37184910-F997D58F-2363-4DF7-8000-17534B116EBA
main subject	mitochondrion deafness mitochondrial DNA
PubMed ID	wds:Q37184910-817C8E96-8E51-40DF-92CA-169CBF201681
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18537605
PubMed ID	18537605
published in	wds:Q37184910-801F0840-B07D-4F83-A0EB-E8E941330924
published in	Current Medicinal Chemistry
issue	wds:Q37184910-5FE0934F-4D36-4916-A7DB-0593C8D773E2
volume	wds:Q37184910-1796F750-37ED-4BBF-9891-D3AF309EDD80
issue	13
volume	15
DOI	wds:Q37184910-C79D9E5D-DD1D-4D5A-8AA0-49F7CD701DAC
DOI	http://dx.doi.org/10.2174/092986708784534910
DOI	10.2174/092986708784534910
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37184910
is cites work of	Mitochondrial dysfunction: a neglected component of skin diseases Complete mitochondrial genomes reveal neolithic expansion into Europe The role of mitochondrial DNA mutations in hearing loss Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients. Disorders of Keratinization Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases Mitochondrial DNA 11777C>A mutation associated Leigh syndrome: case report with a review of the previously described pedigrees Mitochondria in skin health, aging, and disease
is cites work of	wds:Q34046457-9A50F663-3EE2-46C9-A60A-67A501EBB150 wds:Q50433773-76BD0D03-C504-4725-9C27-E2DB1542D778 wds:Q34199844-01CF27C1-D546-4A3D-991D-ADE05CFD2E3B wds:Q38100717-8D300AC7-B776-4697-8836-3504F18F4F05 wds:Q58859701-3466D45B-DAB2-4D08-977D-F683CBC61C54 wds:Q96229607-9F413596-7ACC-4899-AFA2-AE81B427898C wds:Q30458147-8A038AC1-5A7D-408F-88C1-B2A6EA873443 wds:Q38224847-2779A8B1-9DC8-4764-8836-CCE4BF76E2BA wds:Q33587719-F67D99D8-DAD8-46F5-A3B6-FA308F64027B

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