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Characterization of a Spontaneous, Recessive, Missense Mutation Arising in the Tecta Gene
The TECTA gene encodes alpha-tectorin (TECTA), a major noncollagenous component of the tectorial membrane (TM). In humans, mutations in TECTA lead to either dominant (DFNA8/A12) or recessive (DFNB21) forms of nonsyndromic hearing loss. All missense mutations in TECTA that have been reported thus far...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2504605/ https://ncbi.nlm.nih.gov/pubmed/18452040 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10162-008-0116-0 |
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