Toshiyuki Yamamoto
   Department   School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine
   Position   Professor
Article types Case report
Language English
Peer review Peer reviewed
Title A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria
Journal Formal name:Intractable Rare Disease Research
Abbreviation:Intractable Rare Dis Res
ISSN code:2186-361X
Domestic / ForeginForegin
Volume, Issue, Page 6(2),pp.132-136
Author and coauthor Matsumaru S, Oguni H, Ogura H, Shimojima k, Nagata S, Kanno H, Yamamoto T.
Publication date 2017/05
DOI 10.5582/irdr.2017.01020