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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

✍ Scribed by Mariko Yagi; Tomoko Lee; Hiroyuki Awano; Masahiro Tsuji; Go Tajima; Hironori Kobayashi; Yuki Hasegawa; Seiji Yamaguchi; Yasuhiro Takeshima; Masafumi Matsuo


Book ID
116989462
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
220 KB
Volume
104
Category
Article
ISSN
1096-7192

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