Connexin-26 mutations in sporadic and inherited sensorineural deafness-Reference-Cited by-同舟云学术

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Connexin-26 mutations in sporadic and inherited sensorineural deafness

Published:1998-02 Issue:9100 Volume:351 Page:394-398
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Estivill Xavier,Fortina Paolo,Surrey Saul,Rabionet Raquel,Melchionda Salvatore,D'Agruma Leonardo,Mansfield Elaine,Rappaport Eric,Govea Nancy,Milà Montse,Zelante Leopoldo,Gasparini Paolo

Publisher

Elsevier BV

Subject

General Medicine

Reference27 articles.

1. Hearing loss;Nadol;N Engl J Med,1993

2. Epidemiology, aetiology and genetic patterns;Cohen,1995

3. Nonsyndromic hearing impairment: unparalleled heterogeneity;van Camp;Am J Hum Genet,1997

4. Genes responsible for human hereditary deafness: symphony of a thousand;Petit;Nat Genet,1996

5. Connexin-26 mutations in hereditary non-syndromic sensorineural deafness;Kelsell;Nature,1997

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