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.
Journal:
Clinical Endocrinology

ISSN: 0300-0664 1365-2265

Year of publication: 2006

Volume: 64

Issue: 3

Pages: 330-336

Type: Article

DOI: 10.1111/J.1365-2265.2006.02465.X GOOGLE SCHOLAR