학술논문
Detection of the 35de1G/GJB2 and del(GJB6-D 13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing loss
Document Type
Clinical report
Author
Source
Genetic Testing. December 2007, Vol. 11 Issue 4, p347, 6 p.
Subject
Language
English
ISSN
1090-6576
Abstract
Severe to profound hearing impairment affects 1 of every 1000 newborn children each year. Inheritance accounts for 60% of these cases, of which 70% are nonsyndromic. The most common cause [...]