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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Weil, D, Levy, G, Sahly, I, Levi-Acobas, F, Blanchard, S, El-Amraoui, A, Crozet, F, Philippe, H, Abitbol, M, Petit, C
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1996
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC39588/
https://ncbi.nlm.nih.gov/pubmed/8622919
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia