Article
A Japanese adult form of CPT II deficiency associated with a homozygous F383Y mutation.
Neurology - 21 Aug 2007
Aoki J, Yasuno T, Sugie H, Kido H, Nishino I, Shigematsu Y, Kanazawa M, Takayanagi M, Kumami M, Endo K, Kaneoka H, Yamaguchi M, Fukuda T, Yamamoto T
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