Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis-Reference-Cited by-同舟云学术

Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis

Published:2009-10 Issue:10 Volume:30 Page:1419-1427
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Bitoun Marc,Durieux Anne-Cécile,Prudhon Bernard,Bevilacqua Jorge A.,Herledan Adrien,Sakanyan Vehary,Urtizberea Andoni,Cartier Luis,Romero Norma B.,Guicheney Pascale

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21086/fullpdf

Reference41 articles.

1. The role of phosphatidic acid in the regulation of the Ras/MEK/Erk signaling cascade;Andresen;FEBS Lett,2002

2. Mutations in dynamin 2 cause dominant centronuclear myopathy;Bitoun;Nat Genet,2005

3. Dynamin 2 mutations cause sporadic centronuclear myopathy with neonatal onset;Bitoun;Ann Neurol,2007

4. A novel mutation in the dynamin 2 gene in a Charcot-Marie-Tooth type 2 patient: clinical and pathological findings;Bitoun;Neuromuscul Disord,2008

5. A new centronuclear myopathy phenotype due to a novel Dynamin 2 mutation;Bitoun;Neurology,2009

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