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Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1

Mutations of the inositol 5′ phosphatase oculocerebrorenal syndrome of Lowe (OCRL) give rise to the congenital X-linked disorders oculocerebrorenal syndrome of Lowe and Dent disease, two conditions giving rise to abnormal kidney proximal tubule reabsorption, and additional nervous system and ocular...

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Détails bibliographiques
Auteurs principaux: Swan, Laura E., Tomasini, Livia, Pirruccello, Michelle, Lunardi, Joël, De Camilli, Pietro
Format: Artigo
Langue:Inglês
Publié: National Academy of Sciences 2010
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2840420/
https://ncbi.nlm.nih.gov/pubmed/20133602
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0914658107
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