YAMAMOTO Toshiyuki
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 / Foregin | Foregin |
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 |