Publication: A rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletions
| dc.contributor.author | Suravee Sroymora | en_US |
| dc.contributor.author | Sumalee Jindadamrongwech | en_US |
| dc.contributor.author | Punnee Butthep | en_US |
| dc.contributor.author | Suporn Chuncharunee | en_US |
| dc.contributor.other | Faculty of Medicine, Ramathibodi Hospital, Mahidol University | en_US |
| dc.contributor.other | Mahidol University | en_US |
| dc.date.accessioned | 2018-06-11T04:37:57Z | |
| dc.date.available | 2018-06-11T04:37:57Z | |
| dc.date.issued | 2012-04-01 | en_US |
| dc.description.abstract | A large deletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai woman with Hb H disease. The proband has α-thal-1 (SEA type) in conjunction with a 16.6 kb deletion affecting the α2-globin allele. The proband had severe anemia and required a blood transfusion during puerperium. © 2012 Informa Healthcare USA, Inc. | en_US |
| dc.identifier.citation | Hemoglobin. Vol.36, No.2 (2012), 200-204 | en_US |
| dc.identifier.doi | 10.3109/03630269.2012.655355 | en_US |
| dc.identifier.issn | 1532432X | en_US |
| dc.identifier.issn | 03630269 | en_US |
| dc.identifier.other | 2-s2.0-84858144713 | en_US |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/13764 | |
| dc.rights | Mahidol University | en_US |
| dc.rights.holder | SCOPUS | en_US |
| dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84858144713&origin=inward | en_US |
| dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
| dc.subject | Medicine | en_US |
| dc.title | A rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletions | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84858144713&origin=inward | en_US |