The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically

BACKGROUND: Mutations in the gene for Usher syndrome 2A (USH2A) are causative for non-syndromic retinitis pigmentosa and Usher syndrome, a condition that is the most common cause of combined deaf-blindness. To gain insight into the molecular pathology underlying USH2A-associated retinal degeneration...

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Detalles Bibliográficos
Autores principales: Kersten, Ferry FJ, van Wijk, Erwin, Hetterschijt, Lisette, Bauβ, Katharina, Peters, Theo A, Aslanyan, Mariam G, van der Zwaag, Bert, Wolfrum, Uwe, Keunen, Jan EE, Roepman, Ronald, Kremer, Hannie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3541543/
https://www.ncbi.nlm.nih.gov/pubmed/23351521
http://dx.doi.org/10.1186/2046-2530-1-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3541543/
https://www.ncbi.nlm.nih.gov/pubmed/23351521
http://dx.doi.org/10.1186/2046-2530-1-2

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