✦ LIBER ✦
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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