Dominantly Inherited Cytoplasmic Body Myopathy in a Japanese Kindred.
Author:
Affiliation:
1. Department of Neurology
2. Department of Pathology, Tohoku University School of Medicine
Publisher
Tohoku University Medical Press
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
http://www.jstage.jst.go.jp/article/tjem1920/170/4/170_4_261/_pdf
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Hereditary myopathy with early respiratory failure (HMERF): Still rare, but common enough;Neuromuscular Disorders;2018-03
2. Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure;Journal of Neurology, Neurosurgery & Psychiatry;2013-03-13
3. Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure;Journal of Human Genetics;2013-02-28
4. Titin mutation segregates with hereditary myopathy with early respiratory failure;Brain;2012-05-09
5. Hereditary Myopathies;Elextrodiagnostic Medicine;2002
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