Kijima Kazuki | Department Of Pediatrics Yamagata University School Of Medicine

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著作論文

Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
Periaxin mutation in Japanese patients with Charcot-Marie-Tooth disease
Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease
Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan

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