对患有甲状腺失调和TSH受体 (TSHR) 缺陷的患者进行遗传和功能研究

Diego Yeste1,2,3, Noelia Baz-Redón1,2, María Antolín4

  • 1Growth and Development Group, Vall d'Hebron Institut de Recerca (VHIR)-Pediatric Endocrinology Section, Hospital Universitari Vall d'Hebron (HUVH), 08035 Barcelona, Spain.

概括

在TSH受体 (TSHR) 的遗传缺陷导致甲状腺问题. 这项研究在五名患者中发现了六种TSHR变异,证实了它们的致病性,并改善了甲状腺失调和失调激素发生的基因型-表型相关性.

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