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Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next‐generation sequencing
BACKGROUND: Nonsyndromic hearing loss (NSHL) is the most common sensorineural disorder and one of the most common human defects. Autosomal recessive inheritance accounts for a huge percentage of familial cases. Next‐generation sequencing (NGS) is a powerful molecular diagnostic strategy for NSHL. Th...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6687625/ https://ncbi.nlm.nih.gov/pubmed/31250571 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.808 |
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