| 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 |
| Gene_locus related to this paper: human-TG |
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
Citterio CE, Coutant R, Rouleau S, Miralles Garcia JM, Gonzalez-Sarmiento R, Rivolta CM, Targovnik HM (2011)
Clinical Endocrinology (Oxf)
74 :533