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Hisahide Nishio
Hisahide Nishio
Boston Children's Hospital
Mutation
Genetics
Biology
Missense mutation
Endocrinology
3
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26
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Germ-line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion
2008
Pediatrics International
Ahmad Hamim Sadewa
Teguh Haryo Sasongko
Myeong Jin Lee
Kazunari Daikoku
Akiyo Yamamoto
Takemi Yamasaki
Shigenori Tanaka
Masafumi Matsuo
Hisahide Nishio
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Citations (23)
CLINICAL CASE SEMINAR Somatic and Germline Mosaicism for a Mutation of the PHEX Gene Can Lead to Genetic Transmission of X-Linked Hypophosphatemic Rickets That Mimics an Autosomal Dominant Trait
2006
The Journal of Clinical Endocrinology and Metabolism
Katsumi Goji
Kayo Ozaki
Ahmad Hamim Sadewa
Hisahide Nishio
Masafumi Matsuo
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Citations (3)
ITAI-ITAI DISEASE AND CADMIUM TOXICITY
2002
Hisahide Nishio
Myeong Jin Lee
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