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Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Kurima, Kiyoto; Peters, Linda M; Yang, Yandan; Riazuddin, Saima; Ahmed, Zubair M; Naz, Sadaf; Arnaud, Deidre; Drury, Stacy; Mo, Jianhong; Makishima, Tomoko; Ghosh, Manju; Menon, P S N; Deshmukh, Dilip; Oddoux, Carole; Ostrer, Harry; Khan, Shaheen; Riazuddin, Sheikh; Deininger, Prescott L; Hampton, Lori L; Sullivan, Susan L; Battey, James F; Keats, Bronya J B; Wilcox, Edward R; Friedman, Thomas B; Griffith, Andrew J.
Affiliation
  • Kurima K; Section on Gene Structure and Function, Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, Maryland 20850, USA.
Nat Genet ; 30(3): 277-84, 2002 Mar.
Article in En | MEDLINE | ID: mdl-11850618
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Collection: 01-internacional Database: MEDLINE Main subject: Deafness / Genes, Dominant / Genes, Recessive / Hair Cells, Auditory / Mutation Limits: Animals / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2002 Document type: Article Affiliation country: United States Country of publication: United States
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Deafness / Genes, Dominant / Genes, Recessive / Hair Cells, Auditory / Mutation Limits: Animals / Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2002 Document type: Article Affiliation country: United States Country of publication: United States