A patient with mitochondrial trifunctional protein deficiency due to the mutations in the HADHB gene showed recurrent myalgia since early childhood and was diagnosed in adolescence.
A patient with mitochondrial trifunctional protein deficiency due to the mutations in the HADHB gene showed recurrent myalgia since early childhood and was diagnosed in adolescence.
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DOI：
10.1016/j.ymgme.2011.09.025
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发表时间：
2011-12
影响因子：
3.8
通讯作者：
M. Yagi;Tomoko Lee;H. Awano;M. Tsuji;G. Tajima;Hironori Kobayashi;Y. Hasegawa;S. Yamaguchi;Y. Takeshima;M. Matsuo
中科院分区：
文献类型：
--
作者：
M. Yagi;Tomoko Lee;H. Awano;M. Tsuji;G. Tajima;Hironori Kobayashi;Y. Hasegawa;S. Yamaguchi;Y. Takeshima;M. Matsuo
