Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations-Reference-Cited by-同舟云学术

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

Published:2009-05 Issue:5 Volume:73 Page:699-705
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Sırmacı Aslı,Duman Duygu,Öztürkmen-Akay Hatice,Erbek Seyra,İncesulu Armağan,Öztürk-Hişmi Burcu,Arıcı Z. Serap,Yüksel-Konuk E. Berrin,Taşır-Yılmaz Seda,Tokgöz-Yılmaz Suna,Cengiz Filiz Başak,Aslan İdil,Yıldırım Müzeyyen,Hasanefendioğlu-Bayrak Aylin,Ayçiçek Abdullah,Yılmaz İsmail,Fitoz Suat,Altın Fazilet,Özdağ Hilal,Tekin Mustafa

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference14 articles.

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4. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function;Kurima;Nat. Genet.,2002

5. Exact genetic linkage computations for general pedigrees;Fishelson;Bioinformatics,2002

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