Publication:
A new haemoglobin variant: Haemoglobin anantharaj alpha 11 (A9) lysine → glutamic acid

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dc.contributor.authorS. Pootrakulen_US
dc.contributor.authorB. Kematornen_US
dc.contributor.authorS. Na-Nakornen_US
dc.contributor.authorS. Suanpanen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand Ministry of Public Healthen_US
dc.date.accessioned2018-04-19T14:08:58Z
dc.date.available2018-04-19T14:08:58Z
dc.date.issued1975-09-09en_US
dc.description.abstractFour heterozygotes for a fast α-chain variant in a Thai family were detected on starch gel electrophoresis during a survey study on iron deficiency anaemia in a rural area not far from Bangkok. They were healthy and had normal haematological profiles except for the presence of around 44% abnormal pigment, quantitated by cellulose acetate electrophoresis. The structural characterization of the variant by globin chain separation, peptide mapping, and amino acid analyses of the abnormal peptides indicated that lysine residue 11 (A9) of α-chain was replaced by glutamic acid. This mutation has not been previously described and it is proposed that it be called Haemoglobin Anantharaj. © 1975.en_US
dc.identifier.citationBBA - Protein Structure. Vol.405, No.1 (1975), 161-166en_US
dc.identifier.doi10.1016/0005-2795(75)90326-8en_US
dc.identifier.issn00052795en_US
dc.identifier.other2-s2.0-0016743770en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/10803
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0016743770&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleA new haemoglobin variant: Haemoglobin anantharaj alpha 11 (A9) lysine → glutamic aciden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0016743770&origin=inwarden_US

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