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A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria
Matsumaru, Shigeto, Oguni, Hirokazu, Ogura, Hiromi, Shimojima, Keiko, Nagata, Satoru, Kanno, Hitoshi, Yamamoto, ToshiyukiVolume:
6
Year:
2017
Language:
english
Journal:
Intractable & Rare Diseases Research
DOI:
10.5582/irdr.2017.01020
File:
PDF, 828 KB
english, 2017