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Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion

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dc.contributor.authorSergio Ottolenghien_US
dc.contributor.authorW. George Lanyonen_US
dc.contributor.authorJohn Paulen_US
dc.contributor.authorRobert Williamsonen_US
dc.contributor.authorD. J. Weatherallen_US
dc.contributor.authorJ. B. Cleggen_US
dc.contributor.authorJon Pritcharden_US
dc.contributor.authorS. Pootrakulen_US
dc.contributor.authorWong Hock Boonen_US
dc.contributor.otherBeatson Institute for Cancer Researchen_US
dc.contributor.otherUniversity of Liverpoolen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity ofen_US
dc.date.accessioned2018-04-19T13:59:52Z
dc.date.available2018-04-19T13:59:52Z
dc.date.issued1974-12-01en_US
dc.description.abstractTwo independent groups show that the absence of all or part of the globin α-chain gene is the origin of the homozygous α thalassaemia. © 1974 Nature Publishing Group.en_US
dc.identifier.citationNature. Vol.251, No.5474 (1974), 389-392en_US
dc.identifier.doi10.1038/251389a0en_US
dc.identifier.issn00280836en_US
dc.identifier.other2-s2.0-0016228694en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/10731
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0016228694&origin=inwarden_US
dc.subjectMultidisciplinaryen_US
dc.titleGene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0016228694&origin=inwarden_US

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