Rapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia

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dc.contributor.authorAbali, Saygin
dc.contributor.authorAbali, Zehra Yavas
dc.contributor.authorYararbas, Kanay
dc.contributor.authorSemiz, Serap
dc.date.accessioned2025-10-16T15:18:48Z
dc.date.issued2021
dc.identifier.doi10.1515/jpem-2021-0087
dc.identifier.otherWOS:000694009200017
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/7217
dc.publisherWALTER DE GRUYTER GMBH
dc.sourceJOURNAL OF PEDIATRIC ENDOCRINOLOGY \& METABOLISM
dc.subjectALB gene
dc.subjectalbumin
dc.subjectfamilial dysalbuminemic hyperthyroxinemia
dc.subjecthyperthyroxinemia
dc.subjectthyroid hormone resistance
dc.titleRapid molecular diagnosis of ALB gene variants prevents unnecessary interventions in familial dysalbuminemic hyperthyroxinemia
dc.typeArticle

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