Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study-Reference-Cited by-同舟云学术

Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study

Published:2003-12 Issue:6 Volume:73 Page:1452-1458
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

del Castillo Ignacio,Moreno-Pelayo Miguel A.,del Castillo Francisco J.,Brownstein Zippora,Marlin Sandrine,Adina Quint,Cockburn David J.,Pandya Arti,Siemering Kirby R.,Chamberlin G. Parker,Ballana Ester,Wuyts Wim,Maciel-Guerra Andréa Trevas,Álvarez Araceli,Villamar Manuela,Shohat Mordechai,Abeliovich Dvorah,Dahl Hans-Henrik M.,Estivill Xavier,Gasparini Paolo,Hutchin Tim,Nance Walter E.,Sartorato Edi L.,Smith Richard J.H.,Van Camp Guy,Avraham Karen B.,Petit Christine,Moreno Felipe

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference21 articles.

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3. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment;del Castillo;N Engl J Med,2002

4. A comprehensive genetic map of the human genome based on 5,264 microsatellites;Dib;Nature,1996

5. Connexins, connexons, and intercellular communication;Goodenough;Annu Rev Biochem,1996

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