About: Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

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About: Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	articolo scientifico (it) artículu científicu espublizáu en 1998 (ast) vědecký článek publikovaný v roce 1998 (cs) vedecký článok (publikovaný 1998/11/01) (sk) مقالة علمية (نشرت في نوفمبر 1998) (ar) 1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в листопаді 1998 (uk) 1998 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) article scientifique publié en 1998 (fr) scientific journal article (en) wetenschappelijk artikel (gepubliceerd op 1998/11/01) (nl) im November 1998 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28117054-AACD3085-0E7D-4994-9116-E620FD1246F6
publication date	1998-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28117054-A068CC29-E237-4661-86B2-F14DB2CF0F70
language of work or name	English
cites work	wds:Q28117054-0178096B-06DB-4A42-A8C0-FCD94C067E7B wds:Q28117054-0883DA4B-8509-4F99-B388-B66FF7EB3416 wds:Q28117054-0DF4ED8C-1A89-4E88-8492-509F0313D32C wds:Q28117054-19445CC9-D047-4CE8-A6A4-810037591DAF wds:Q28117054-1E775958-A947-4273-96D5-DE611CB9CE29 wds:Q28117054-2B9460C5-C663-49AC-994C-7595037B4B8E wds:Q28117054-2C19CA50-F3F1-4172-B981-D99954A7D2C6 wds:Q28117054-2ED057E0-73A8-443F-9ECC-25ECF424A2DC wds:Q28117054-39DD1776-BB39-4EB5-BA88-0C3F04E30357 wds:Q28117054-48746FF2-FCFD-4915-B105-8543BB5A4279 wds:Q28117054-5005DAB4-4EF7-4450-AFEF-9A7DF94A1D21 wds:Q28117054-6598B09D-D16E-4680-9139-C674FC864223 wds:Q28117054-65FFEB9D-A7E0-4743-AD18-D4CAA655378C wds:Q28117054-70EB1352-90E5-46B1-BAE4-2AA89463A264 wds:Q28117054-76F6B537-5C8F-44F6-859F-DD115652F9AD wds:Q28117054-8E5EF887-F140-425E-8668-470078114E56 wds:Q28117054-AFCF351A-5448-40C7-B8D9-B3439D6C9AE1 wds:Q28117054-B0B4B46D-1BB1-4C04-9712-7A4E36CE8191 wds:Q28117054-BC5E0D57-685B-4A87-8473-326C33DF017B wds:Q28117054-BDB1089C-A701-484E-9AC1-07FC8D7991C8 wds:Q28117054-C1497896-E515-416F-ABEE-B448AA88BE02 wds:Q28117054-CAD794FD-EAE5-452A-BB31-F962055DEDFA wds:Q28117054-D303C18B-2363-49E3-B835-CB3F8345957F wds:Q28117054-EFC7D215-3ECF-45B4-998D-F5D62318EAC5
cites work	Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous Connexin 26 mutations in hereditary non-syndromic sensorineural deafness Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Mutations in the myosin VIIA gene cause non-syndromic recessive deafness The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene A mutation in PDS causes non-syndromic recessive deafness A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes Genes responsible for human hereditary deafness: symphony of a thousand Connexin 26 gene linked to a dominant deafness. Basic local alignment search tool Molecular mechanism of hemolymph clotting system in Limulus A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13 Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9 Autosomal dominant sensorineural hearing loss. Further temporal bone findings Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Type A modules: interacting domains found in several non-fibrillar collagens and in other extracellular matrix proteins Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss Missense mutation in the pore region of HERG causes familial long QT syndrome Intracellular serine-protease zymogen, factor C, from horseshoe crab hemocytes. Its activation by synthetic lipid A analogues and acidic phospholipids Connexin mutations and hearing loss.
author name string	wds:Q28117054-0ED574C3-B434-4AC0-B4B5-90AB7A6E13AC wds:Q28117054-3DE62AF1-4B89-42A6-B72F-E37A11E461A4 wds:Q28117054-418CF751-B43C-48BA-88A5-DD10A5935772 wds:Q28117054-4321E8D5-5222-4AA9-836C-BD3259958AC6 wds:Q28117054-4EFD1B9D-1E40-4F56-B3CC-0B50D5A03E0E wds:Q28117054-75B8DAA9-A352-4BA8-86CF-712BD2659CD4 wds:Q28117054-9F3FAFF3-9BB9-4569-AD80-70DB8605EC05 wds:Q28117054-A2D248DD-3C8F-4EEF-B323-FD299AE466AF wds:Q28117054-B5DEBB48-AA9A-4938-B9AA-A8F700C6A568 wds:Q28117054-C424C099-E350-47D3-9B9D-126F00F20DCF wds:Q28117054-CC10E3E5-A585-4B49-9B3C-7D06DE5347B8 wds:Q28117054-DAFB753A-4A90-4436-981D-B1F46989775E wds:Q28117054-F151B698-8DDC-4036-8DF4-8C6DB4AA1AF1
OpenCitations bibliographic resource ID	wds:Q28117054-19D6B718-75BC-4084-933A-0AD8BD49CA33
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/2286139
author name string	L. Lu C. E. Seidman C. C. Morton J. B. Nadol S. Heller F. H. Linthicum A. J. Hudspeth M. McKenna R. D. Eavey N. G. Robertson J. F. Lubianca Neto R. T. Miyamoto S. N. Merchant
OpenCitations bibliographic resource ID	2286139
rdfs:label	Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction (en) Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction (nl) Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction (ast)
skos:prefLabel	Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction (en) Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction (nl) Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction (ast)

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