Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases-Reference-Cited by-同舟云学术

Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases

Published:2016-03 Issue:3 Volume:38 Page:293-301
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Yamada Kenji,Kobayashi Hironori,Bo Ryosuke,Takahashi Tomoo,Purevsuren Jamiyan,Hasegawa Yuki,Taketani Takeshi,Fukuda Seiji,Ohkubo Takuya,Yokota Takanori,Watanabe Mutsufusa,Tsunemi Taiji,Mizusawa Hidehiro,Takuma Hiroshi,Shioya Ayako,Ishii Akiko,Tamaoka Akira,Shigematsu Yosuke,Sugie Hideo,Yamaguchi Seiji

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Ministry of Health, Labor and Welfare

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

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3. Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency);Goodman;J Inherit Metab Dis,1984

4. Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts;Frerman;Proc Natl Acad Sci USA,1985

5. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings;Lehnert;Eur J Pediatr,1982

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