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The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report
BACKGROUND: Many mutations in the α-tectorin gene (TECTA) have been reported to cause non-syndromic hearing loss (NSHL) in either a dominant or recessive inheritance pattern. Among the identified TECTA mutations, H1400Y has been associated with NSHL in two independent studies. However, its exact rol...
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| Publicat a: | BMC Med Genet |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6444877/ https://ncbi.nlm.nih.gov/pubmed/30935366 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0775-1 |
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