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Paper Report for: Citterio_2011_Clin.Endocrinol.(Oxf)_74_533

Reference

Title: A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism
Citterio CE, Coutant R, Rouleau S, Miralles Garcia JM, Gonzalez-Sarmiento R, Rivolta CM, Targovnik HM
Ref: Clinical Endocrinology (Oxf), 74:533, 2011 : PubMed

        



Related information

Gene_Locus| human-TG
Mutation | R296X_human-TG,



Citations formats

Citterio CE, Coutant R, Rouleau S, Miralles Garcia JM, Gonzalez-Sarmiento R, Rivolta CM, Targovnik HM (2011)
A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism
Clinical Endocrinology (Oxf) 74: 533-5

Citterio CE, Coutant R, Rouleau S, Miralles Garcia JM, Gonzalez-Sarmiento R, Rivolta CM, Targovnik HM (2011)
Clinical Endocrinology (Oxf) 74: 533-5



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