High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect

1. Loidi, L.
2. Quinteiro, C.
3. Parajes, S.
4. Barreiro, J.
5. Lestón, D.G.
6. Cabezas-Agrícola, J.M.
7. Sueiro, A.M.
8. Araujo-Vilar, D.
9. Catro-Feijóo, L.
10. Costas, J.
11. Pombo, M.
12. Domínguez, F.