Elevated urinary β2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagy-Reference-Cited by-同舟云学术

Elevated urinary β2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagy

Published:2013-11 Issue:11 Volume:23 Page:911-916
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Kurashige Takashi,Takahashi Tetsuya,Yamazaki Yu,Nagano Yoshito,Kondo Keita,Nakamura Takeshi,Yamawaki Takemori,Tsuburaya Rie,Hayashi Yukiko K.,Nonaka Ikuya,Nishino Ichizo,Matsumoto Masayasu

Publisher

Elsevier BV

Subject

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

Reference13 articles.

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4. Ramachandran N, Munteanu I, Wang P et al. VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy. Acta Neuropathol (in press).

5. Vacuolar ATPases: rotary proton pumps in physiology and pathophysiology;Forgac;Nat Rev Mol Cell Biol,2007

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