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A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss
BACKGROUND: Hearing loss is a heterogeneous neurosensory disorder. Mutations of 56 genes are reported to cause recessively inherited nonsyndromic deafness. OBJECTIVE: We sought to identify the genetic lesion causing hearing loss segregating in a large consanguineous Pakistani family. METHODS AND RES...
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| Publicat a: | J Med Genet |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4529444/ https://ncbi.nlm.nih.gov/pubmed/25941349 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2015-103023 |
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