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Identification of four TMC1 variations in different Chinese families with hereditary hearing loss
BACKGROUND: Variants in TMC1 (transmembrane channel‐like 1) can cause both autosomal dominant and recessive hearing loss in human population. Mice with Tmc1 variants have been shown to be ideal animal models for gene therapy. In this article, we report four TMC1 variants in four different Chinese fa...
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| Vydáno v: | Mol Genet Genomic Med |
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| Hlavní autoři: | , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6081220/ https://ncbi.nlm.nih.gov/pubmed/29654653 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.394 |
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