A mutation in hnRNPA1 causes isolated inclusion body myopathy in two families with multisystem proteinopathy
A mutation in hnRNPA1 causes isolated inclusion body myopathy in two families with multisystem proteinopathy
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hnRNPA1 突变导致两个多系统蛋白病家族出现孤立性包涵体肌病
DOI：
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发表时间：
2015
期刊：
影响因子：
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通讯作者：
Aoki M.
中科院分区：
文献类型：
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作者：
Izumi R;Warita H;Niihori T;Takahashi T;Tateyama M;Suzuki N;Nishiyama A;Shirota M;Funayama R;Nakayama K;Mitsuhashi S;Nishino I;Aoki Y;Aoki M.
