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Shigeto Matsumaru
Shigeto Matsumaru
PGK deficiency
Genetics
Immunology
Hemolytic anemia
Intellectual disability
2
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8
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0
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A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria
2017
Intractable & Rare Diseases Research
Shigeto Matsumaru
Hirokazu Oguni
Hiromi Ogura
Keiko Shimojima
Satoru Nagata
Hitoshi Kanno
Toshiyuki Yamamoto
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Symptomatic epilepsy with chromosome aberration: report of two cases
2017
Shigeto Matsumaru
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