A Japanese adult form of CPT II deficiency associated with a homozygous F383Y mutation.
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.
Aoki J, et al. Among authors: kido h.
Neurology. 2007 Aug 21;69(8):804-6. doi: 10.1212/01.wnl.0000267665.44477.85.
Neurology. 2007.
PMID: 17709715
No abstract available.