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GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss
BACKGROUND: A substantial amount of nuclear genes have been identified to be implicated in genetic hearing loss, while X-linked hearing loss is genetically heterogeneous and relatively infrequent. OBJECTIVE: To identify the causative gene mutation in a five-generation Chinese family with an X-linked...
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| Publicado no: | J Med Genet |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5502311/ https://ncbi.nlm.nih.gov/pubmed/28096187 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2016-104320 |
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