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Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke‐like episodes syndrome and NADH‐CoQ reductase deficiency
Author(s) -
Kobayashi M.,
Morishita H.,
Sugiyama N.,
Yokochi K.,
Nakano M.,
Wada Y.,
Hotta Y.,
Terauchi A.,
aka I.
Publication year - 1986
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf01799670
Subject(s) - medical school , medicine , pediatrics , medical education
M. KOBAYASHI 1, H. MORISHITA 1, N. SUGIYAMA 1, K. YOKOCHI 1, M. NAKANO 1, Y. WADA 1, Y. HOTTA 2, A. TERAUCHI 3 and I. NONAKA 4 1Department of Paediatrics and ~First Department of Anatomy, Medical School, Nagoya City University, Kawasumi-cho, Mizuho-ku, Nagoya 467, Japan 3Higashimatsumoto National Sanatorium, Matsumoto 399-65, Nagano, Japan 4National Centre for Nervous, Mental and Muscular Disorders, Kodaira 187, Tokyo, Japan