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Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.

The gene encoding human myosin VIIA is responsible for Usher syndrome type III (USH1B), a disease which associates profound congenital sensorineural deafness, vestibular dysfunction, and retinitis pigmentosa. The reconstituted cDNA sequence presented here predicts a 2215 amino acid protein with a ty...

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Bibliografske podrobnosti
izdano v:Proc Natl Acad Sci U S A
Principais autores: Weil, D, Levy, G, Sahly, I, Levi-Acobas, F, Blanchard, S, El-Amraoui, A, Crozet, F, Philippe, H, Abitbol, M, Petit, C
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 1996
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC39588/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8622919/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.93.8.3232
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