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Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus

✍ Scribed by Sadaf Naz; Chantal M. Giguere; David C. Kohrman; Kristina L. Mitchem; Saima Riazuddin; Robert J. Morell; Arabandi Ramesh; Srikumari Srisailpathy; Dilip Deshmukh; Sheikh Riazuddin; Andrew J. Griffith; Thomas B. Friedman; Richard J.H. Smith; Edward R. Wilcox


Book ID
117853981
Publisher
American Society of Human Genetics
Year
2002
Tongue
English
Weight
292 KB
Volume
71
Category
Article
ISSN
0002-9297

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## Communicated by Henrik Dahl Approximately 80% of hereditary hearing loss is non-syndromic. Non-syndromic deafness is the most genetically heterogeneous trait. The most common and severe form of hereditary hearing impairment is autosomal recessive non-syndromic hearing loss (ARNSHL), accounting f