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, C.E.
- Coutant, R.
- Rouleau, S.
- Miralles García, J.M.
- Gonzalez-Sarmiento, R.
- Rivolta, C.M.
- Targovnik, H.M.
ISSN: 0300-0664, 1365-2265
Year of publication: 2011
Volume: 74
Issue: 4
Pages: 533-535
Type: Letter