Report for Chabardes B

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References (1)

Title : Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-->A [R2223H]) resulting in fetal goitrous hypothyroidism - Caron_2003_J.Clin.Endocrinol.Metab_88_3546

Author(s) : Caron P , Moya CM , Malet D , Gutnisky VJ , Chabardes B , Rivolta CM , Targovnik HM

Ref : J Clinical Endocrinology Metab , 88 :3546 , 2003

Abstract : Caron_2003_J.Clin.Endocrinol.Metab_88_3546

ESTHER : Caron_2003_J.Clin.Endocrinol.Metab_88_3546

PubMedSearch : Caron_2003_J.Clin.Endocrinol.Metab_88_3546

PubMedID: 12915634

Gene_locus related to this paper: human-TG

Report for Chabardes B

General

References (1)

1. Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-->A [R2223H]) resulting in fetal goitrous hypothyroidism