C Kissin, C Collombel, P Baltassat, F Freycon, J Cotte. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Binding SitesBlood Protein ElectrophoresisChild, PreschoolChromosome AberrationsChromosome DisordersDihydrolipoamide DehydrogenaseHemeHemoglobins, AbnormalHeterozygoteHistidineHumansMaleMetabolism, Inborn ErrorsMethemoglobin/analysisMethemoglobinemia/congenitalMutationSpectrophotometryTyrosine
Substances: See more » Hemoglobins, AbnormalTyrosineHemeHistidineMethemoglobinDihydrolipoamide Dehydrogenase
Year: 1971 PMID: 4252102
Source DB: PubMed Journal: Nouv Rev Fr Hematol ISSN: 0029-4810