Genetic epidemiological studies of congenital/prelingual deafness in Turkey: Population structure and mating type are major determinants of mutation identification-Reference-Cited by-同舟云学术

Genetic epidemiological studies of congenital/prelingual deafness in Turkey: Population structure and mating type are major determinants of mutation identification

Published:2007-07-15 Issue:14 Volume:143A Page:1583-1591
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Tekin Mustafa,Arıcı Zehra Serap

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference28 articles.

1. Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness

2. Four novelTMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss

3. Mutations in thelipoma HMGIC fusion partner-like 5 (LHFPL5)gene cause autosomal recessive nonsyndromic hearing loss

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