Two compound heterozygous mutations (c.215delA/c.2422T→C and c.387delC/c.1159G→A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect
- Rivolta, C.M.
- Louis-Tisserand, M.
- Varela, V.
- Gruñeiro-Papendieck, L.
- Chiesa, A.
- González-Sarmiento, R.
- Targovnik, H.M.
ISSN: 0300-0664, 1365-2265
Argitalpen urtea: 2007
Alea: 67
Zenbakia: 2
Orrialdeak: 238-246
Mota: Artikulua