Report for Rouleau S

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References (1)

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 -

Author(s) : Citterio CE , Coutant R , Rouleau S , Miralles Garcia JM , Gonzalez-Sarmiento R , Rivolta CM , Targovnik HM

Ref : Clinical Endocrinology (Oxf) , 74 :533 , 2011

PubMedID: 21128992

Gene_locus related to this paper: human-TG

Report for Rouleau S

General

References (1)

1. 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