DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions-Reference-Cited by-同舟云学术

DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions

Published:2013-03 Issue:3 Volume:23 Page:269-276
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Sato Takatoshi,Hayashi Yukiko K.,Oya Yasushi,Kondo Tomoyoshi,Sugie Kazuma,Kaneda Daita,Houzen Hideki,Yabe Ichiro,Sasaki Hidenao,Noguchi Satoru,Nonaka Ikuya,Osawa Makiko,Nishino Ichizo

Funder

Ministry of Health, Labour and Welfare

NCNP

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference18 articles.

1. The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophy;Sandell;J Neurol Neurosurg Psychiatry,2010

2. Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy;Harms;Ann Neurol,2012

3. Mutations affecting the cytoplasmic function of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy;Sarparanta;Nat Genet,2012

4. A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregation;Hageman;Mol Cell,2010

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