Publication:
Hemoglobin dhonburi α<inf>2</inf>β<inf>2</inf>126 (H4) Val → Gly: A new unstable β variant producing a β‐thalassemia intermedia phenotype in association with β°‐Thalassemia

dc.contributor.authorJ. Bardakdjian‐Michauen_US
dc.contributor.authorJ. Delanoe‐Garinen_US
dc.contributor.authorC. Lacombeen_US
dc.contributor.authorY. Blouquiten_US
dc.contributor.authorJ. Riouen_US
dc.contributor.authorF. Galacterosen_US
dc.contributor.authorS. Fucharoenen_US
dc.contributor.authorP. Winichagoonen_US
dc.contributor.authorP. Wasien_US
dc.contributor.authorJ. Kisteren_US
dc.contributor.otherHopital Henri Mondoren_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherInsermen_US
dc.date.accessioned2018-06-14T09:26:15Z
dc.date.available2018-06-14T09:26:15Z
dc.date.issued1990-01-01en_US
dc.description.abstractWhile investigating the mechanism of a β‐thalassemia intermedia phenotype in a 34 year old Thai male, a new Hb variant β 126 Val → Gly named Hb Dhonburi was discovered. Genetic and structural studies revealed the existence of a β°‐thalassemia genotype in association with the β variant. The new variant is unstable but exhibits normal oxygen binding properties. Hb Dhonburi was also discovered in the mother of the propositus in association with Hb E. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Companyen_US
dc.identifier.citationAmerican Journal of Hematology. Vol.35, No.2 (1990), 96-99en_US
dc.identifier.doi10.1002/ajh.2830350206en_US
dc.identifier.issn10968652en_US
dc.identifier.issn03618609en_US
dc.identifier.other2-s2.0-0025044955en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/16166
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025044955&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleHemoglobin dhonburi α<inf>2</inf>β<inf>2</inf>126 (H4) Val → Gly: A new unstable β variant producing a β‐thalassemia intermedia phenotype in association with β°‐Thalassemiaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0025044955&origin=inwarden_US

Files

Collections