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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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Bibliographische Detailangaben
Hauptverfasser: 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.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2005
Schlagworte:
Online Zugang: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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