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Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14

✍ Scribed by Hui Li; Jia-Xin Wang; Cheng-Ye Wang; Ping Yu; Qiang Zhou; Yong-Gang Chen; Lu-Hang Zhao; Ya-Ping Zhang


Book ID
106134622
Publisher
Springer
Year
2007
Tongue
English
Weight
283 KB
Volume
122
Category
Article
ISSN
0340-6717

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## Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of hereditary hearing impairment (HHI). To date, 16 different loci have been reported, making ARNSHL an extremely heterogeneous disorder. One of these loci, DFNB4, was mapped to a 5-cM interval of 7q31 in a large Midd