Biallelic mutations in the myopalladin gene, MYPN are associated with childhood-onset, slowly progressive nemaline myopathy

被引:0
|
作者
Matsumoto, N. [1 ]
Miyatake, S. [1 ]
机构
[1] Yokohama City Univ, Grad Sch Med, Yokohama, Kanagawa, Japan
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D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
C08.1
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页码:55 / 55
页数:1
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