Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment

To date, 37 genes have been identified for nonsyndromic hearing impairment (NSHI). Identifying the functional sequence variants within these genes and knowing their population-specific frequencies is of public health value, in particular for genetic screening for NSHI. To determine putatively functi...

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Main Authors: Santos, Regie Lyn P., El-Shanti, Hatem, Sikandar, Shaheen, Lee, Kwanghyuk, Bhatti, Attya, Yan, Kai, Chahrour, Maria H., McArthur, Nathan, Pham, Thanh L., Mahasneh, Amjad Abdullah, Ahmad, Wasim, Leal, Suzanne M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2005
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2909111/
https://ncbi.nlm.nih.gov/pubmed/16389551
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00109-005-0015-3
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