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Paper Report for: Caron_2003_J.Clin.Endocrinol.Metab_88_3546

Reference

Title: Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-->A [R2223H]) resulting in fetal goitrous hypothyroidism
Caron P, Moya CM, Malet D, Gutnisky VJ, Chabardes B, Rivolta CM, Targovnik HM
Ref: J Clinical Endocrinology Metab, 88:3546, 2003 : PubMed

        



Related information

Gene_Locus| human-TG
Mutation | Y383TfsX19_human-TG, R2242H_human-TG,



Citations formats

Caron P, Moya CM, Malet D, Gutnisky VJ, Chabardes B, Rivolta CM, Targovnik HM (2003)
Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-->A [R2223H]) resulting in fetal goitrous hypothyroidism
J Clinical Endocrinology Metab 88: 3546-53

Caron P, Moya CM, Malet D, Gutnisky VJ, Chabardes B, Rivolta CM, Targovnik HM (2003)
J Clinical Endocrinology Metab 88: 3546-53



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