Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia
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Date
Journal Title
Journal ISSN
Volume Title
dc.identifier.issn
dc.identifier.doi
10.1515/jpem-2021-0087
dc.identifier.other
WOS:000694009200017
dc.description.volume
dc.description.issue
Publisher
WALTER DE GRUYTER GMBH
DOI
10.1515/jpem-2021-0087