The 60th Annual Meeting of the Japanese Society of Child Neurology

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Poster Presentation

Metabolic diseaseMitochondrial disease/Congenital metabolic disorder

[P20] Metabolic diseaseMitochondrial disease/Congenital metabolic disorder

Thu. May 31, 2018 5:35 PM - 6:05 PM Poster (Convention Hall A)

Chair: Shin Nabatame(Department of Pediatrics, Graduate School of Medicine, Osaka University, Suita, Japan)

[P-114] A case of molybdenum cofactor deficiency identified with MOCS1 mutation

Yu Abe, YU AIHARA, WAKABA ENDO, MITSUGU UEMATSU, SHIGEO KURE (Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan)

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