Department of Pediatrics, Tokyo Women’s Medical University, Tokyo, Japan／Institute of Medical Genetics, Tokyo Women’s Medical University, Tokyo, Japan
Institute of Medical Genetics, Tokyo Women’s Medical University, Tokyo, Japan／Tokyo Women’s Medical University Institute of Integrated Medical Sciences, Tokyo, Japan
Department of Pediatrics, National Hospital Organization Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan
Department of Pediatrics, National Hospital Organization Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan
Department of Pediatrics, National Hospital Organization Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan
Department of Child Neurology, Okayama University School of Medicine, Okayama, Japan
Department of Pediatrics, Tokyo Women’s Medical University, Tokyo, Japan
Institute of Medical Genetics, Tokyo Women’s Medical University, Tokyo, Japan／Tokyo Women’s Medical University Institute of Integrated Medical Sciences, Tokyo, Japan
Compound Heterozygous ALDH7A1 Mutation Causes the Hemi-Allelic Expression in a Patient with Pyridoxine-Dependent Epilepsy
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