About: Connexin-26 mutations in sporadic and inherited sensorineural deafness

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 1998 (ast) vědecký článek publikovaný v roce 1998 (cs) ശാസ്ത്രപ്രബന്ധം (ml) наукова стаття, опублікована в лютому 1998 (uk) 1998 թուականի Փետրուարին հրատարակուած գիտական յօդուած (hyw) 1998 թվականի փետրվարին հրատարակված գիտական հոդված (hy) article publié dans la revue scientifique The Lancet (fr) scientific journal article (en) im Februar 1998 veröffentlichter wissenschaftlicher Artikel (de) wetenschappelijk artikel (gepubliceerd op 1998/02/07) (nl) vedecký článok (publikovaný 1998/02/07) (sk) مقالة علمية (نشرت في 7-2-1998) (ar) научни чланак (објављен 1998/02/07) (sr)
publication date	wds:Q28117673-3442277D-B082-4778-97D6-42975E14B443
publication date	1998-02-07 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28117673-1A90B913-2FE0-4A50-BEA7-848A114AE0D0
language of work or name	English
cites work	wds:Q28117673-0D3A265F-12BD-40C1-8555-949E170D4CB9 wds:Q28117673-1A2E076F-FB12-4DDA-8B0F-36E2735E608F wds:Q28117673-1F893E42-7C60-4EFE-A9A6-96286198F7F8 wds:Q28117673-28B48C9C-6AC5-4BAF-AEF4-4B66C221DB9B wds:Q28117673-38FB0240-B39F-4962-9AF2-53577A0E4D4D wds:Q28117673-48F0D169-8C11-4B2E-BF9B-632E6792DF5A wds:Q28117673-4AF7C295-5BEC-44F4-A0B8-1D0490812EC8 wds:Q28117673-59CB3F90-69C6-421F-850B-6F6B40D2571E wds:Q28117673-5F4C8AEB-FF34-4920-A4CB-78CF546A8811 wds:Q28117673-6BA94E68-62AA-4820-9F4E-42D30A2E8BCA wds:Q28117673-926F8E56-63F3-4C32-B4E3-4F10A4AC4E9E wds:Q28117673-AE22F5E6-BF22-4A7C-B2A0-FA565122FCB9 wds:Q28117673-B4DAB85B-8341-4C6A-847E-EB63C6FF1C1B wds:Q28117673-BF342AF0-992E-4E0E-8462-BF3F5C91D235 wds:Q28117673-EC877860-8080-49D0-9872-F3A7BC06CA38 wds:Q28117673-ED387FA0-4A7F-43E2-B0EF-089523CB4A41 wds:Q28117673-F685FFB6-1011-484C-91D5-78DE8779CFA0 wds:Q28117673-FE2E3C61-97E7-484A-8534-CB9C5C070592 wds:Q28117673-FF599522-1D10-4456-9B22-09B2469AD7D4
cites work	Defective myosin VIIA gene responsible for Usher syndrome type 1B Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous Mixing of connexins in gap junction membrane channels Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis Connexin mutations in X-linked Charcot-Marie-Tooth disease Connexin 26 mutations in hereditary non-syndromic sensorineural deafness Mutations in the myosin VIIA gene cause non-syndromic recessive deafness Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene Genes responsible for human hereditary deafness: symphony of a thousand Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Connexin family of gap junction proteins Hearing Loss Receptor synapses without synaptic ribbons in the cochlea of the cat Synaptic transmission: a bidirectional and self-modifiable form of cell-cell communication Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11-->q12 and mouse chromosome 14D1-E1 by in situ hybridization Tight and gap junctions in a vertebrate inner ear Changes in immunostaining of cochleas with experimentally induced endolymphatic hydrops Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations. Structure--function relationships in gap junctions.
author name string	wds:Q28117673-0FAC6FE2-C0A0-4E44-864B-B27650B71080 wds:Q28117673-14B5905D-1796-499D-81E0-D32BAAB9047A wds:Q28117673-1F555B70-377B-46B6-9E62-3F9B7DD89846 wds:Q28117673-48537880-71FC-4574-87E6-61D881743433 wds:Q28117673-4A80D27E-4B51-4C12-80C0-C8B84166086E wds:Q28117673-8367E132-D7C7-49FF-8783-B76D3CD68E2E wds:Q28117673-96FF0E3C-227B-4E0F-B2C7-2AFC027373A9 wds:Q28117673-A9C3EA80-80AB-43BB-B13D-A5108B15F2FA wds:Q28117673-B4B7FB69-FD89-4A2D-9F45-B99F9B1F1EE5
OpenCitations bibliographic resource ID	wds:Q28117673-934B4940-D77D-4294-8F1E-5E9130BA33D8
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1289885
author name string	S. Surrey P. Gasparini E. Mansfield L. Zelante E. Rappaport P. Fortina L. D'Agruma N. Govea S. Melchionda
OpenCitations bibliographic resource ID	1289885
rdfs:label	Connexin-26 mutations in sporadic and inherited sensorineural deafness (en) Connexin-26 mutations in sporadic and inherited sensorineural deafness (nl) Connexin-26 mutations in sporadic and inherited sensorineural deafness (ast)
skos:prefLabel	Connexin-26 mutations in sporadic and inherited sensorineural deafness (en) Connexin-26 mutations in sporadic and inherited sensorineural deafness (nl) Connexin-26 mutations in sporadic and inherited sensorineural deafness (ast)
name	Connexin-26 mutations in sporadic and inherited sensorineural deafness (en) Connexin-26 mutations in sporadic and inherited sensorineural deafness (nl) Connexin-26 mutations in sporadic and inherited sensorineural deafness (ast)
author	wds:Q28117673-3783C3B4-5866-4432-8A17-1AF6C834C0DE wds:Q28117673-58273717-3BBC-4955-94D8-1720BCCAD633 wds:Q28117673-8447AA46-04CC-4099-8A46-ECFD1AC9E5DC
author	Xavier Estivill i Pallejà Raquel Rabionet Montserrat Milà
title	wds:Q28117673-15DDFAFC-3246-48AB-84F7-2DA8A4B4CA57
title	Connexin-26 mutations in sporadic and inherited sensorineural deafness (en)
page(s)	wds:Q28117673-FF076E97-4405-4230-A499-DAD7081F7E59
page(s)	394–398
instance of	wds:Q28117673-71F90883-7FF8-4EAA-B8CB-4AF53A778C28
instance of	scholarly article
main subject	wds:Q28117673-5F9FF255-24EC-414F-84A8-79C6809728DA
main subject	deafness

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