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Family with centronuclear myopathy as a result of a novel p.R369G DNM 2 mutation
Author(s) -
Toyooka Keiko,
Kubo Kumiko,
Fujimura Harutoshi,
Sakoda Sabro,
Tominaga Kayo,
Nishino Ichizo
Publication year - 2015
Publication title -
neurology and clinical neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
0ISSN - 2049-4173
DOI - 10.1111/ncn3.176
Subject(s) - medicine , ptosis , weakness , facial weakness , heel , congenital myopathy , myopathy , scoliosis , anatomy , muscle biopsy , surgery , biopsy
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