Functional consequences of seven novel mutations in the CYP11B1 gene: Four mutations associated with nonclassic and three mutations causing classic 11β-hydroxylase deficiency

  1. Parajes, S.
  2. Loidi, L.
  3. Reisch, N.
  4. Dhir, V.
  5. Rose, I.T.
  6. Hampel, R.
  7. Quinkler, M.
  8. Conway, G.S.
  9. Castro-Feijóo, L.
  10. Araujo-Vilar, D.
  11. Pombo, M.
  12. Dominguez, F.
  13. Williams, E.L.
  14. Cole, T.R.
  15. Kirk, J.M.
  16. Kaminsky, E.
  17. Rumsby, G.
  18. Arlt, W.
  19. Krone, N.
Revista:
Journal of Clinical Endocrinology and Metabolism

ISSN: 0021-972X,  0021-972X

Ano de publicación: 2010

Volume: 95

Número: 2

Páxinas: 779-788

Tipo: Artigo

DOI: 10.1210/JC.2009-0651 GOOGLE SCHOLAR lock_openAcceso aberto editor
Fonte de datos: Scopus