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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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| Hauptverfasser: | , , , , , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2005
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| 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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