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Paper Report for: Rivolta_2005_J.Clin.Endocrinol.Metab_90_3766

Reference

Title: A new case of congenital goiter with hypothyroidism caused by a homozygous p.R277X mutation in the exon 7 of the thyroglobulin gene: a mutational hot spot could explain the recurrence of this mutation
Rivolta CM, Moya CM, Gutnisky VJ, Varela V, Miralles-Garcia JM, Gonzalez-Sarmiento R, Targovnik HM
Ref: J Clinical Endocrinology Metab, 90:3766, 2005 : PubMed

        



Related information

Gene_Locus| human-TG
Mutation | R296X_human-TG,



Citations formats

Rivolta CM, Moya CM, Gutnisky VJ, Varela V, Miralles-Garcia JM, Gonzalez-Sarmiento R, Targovnik HM (2005)
A new case of congenital goiter with hypothyroidism caused by a homozygous p.R277X mutation in the exon 7 of the thyroglobulin gene: a mutational hot spot could explain the recurrence of this mutation
J Clinical Endocrinology Metab 90: 3766-70

Rivolta CM, Moya CM, Gutnisky VJ, Varela V, Miralles-Garcia JM, Gonzalez-Sarmiento R, Targovnik HM (2005)
J Clinical Endocrinology Metab 90: 3766-70



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