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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chupong Ittiwut | en_US |
dc.contributor.author | Rungrote Natesirinilkul | en_US |
dc.contributor.author | Fuanglada Tongprasert | en_US |
dc.contributor.author | Lalita Sathitsamitphong | en_US |
dc.contributor.author | Chane Choed-amphai | en_US |
dc.contributor.author | Kanda Fanhchaksai | en_US |
dc.contributor.author | Pimlak Charoenkwan | en_US |
dc.contributor.author | Kanya Suphapeetiporn | en_US |
dc.contributor.author | Vorasuk Shotelersuk | en_US |
dc.date.accessioned | 2018-11-29T07:54:20Z | - |
dc.date.available | 2018-11-29T07:54:20Z | - |
dc.date.issued | 2018-01-01 | en_US |
dc.identifier.issn | 13652141 | en_US |
dc.identifier.issn | 00071048 | en_US |
dc.identifier.other | 2-s2.0-85053051054 | en_US |
dc.identifier.other | 10.1111/bjh.15559 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053051054&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/62841 | - |
dc.subject | Medicine | en_US |
dc.title | Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | British Journal of Haematology | en_US |
article.stream.affiliations | Chulalongkorn University | en_US |
article.stream.affiliations | King Chulalongkorn Memorial Hospital, Faculty of Medicine Chulalongkorn University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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