A novel missense mutation of RYR1 in familial idiopathic hyper CK-emia-Reference-Cited by-同舟云学术

A novel missense mutation of RYR1 in familial idiopathic hyper CK-emia

Published:2015-09 Issue:1-2 Volume:356 Page:142-147
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Sano Ken,Miura Shiroh,Fujiwara Toshiya,Fujioka Ryuta,Yorita Akiko,Noda Kazuhito,Kida Hiroshi,Azuma Koichi,Kaieda Shinjiro,Yamamoto Ken,Taniwaki Takayuki,Fukumaki Yasuyuki,Shibata Hiroki

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference35 articles.

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4. Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2;Merlini;Muscle Nerve,2005

5. Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle;Prelle;J. Neurol. Sci.,1996

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