High frequency of copy number variations and sequence variants at CYP21A2 locus: Implication for the genetic diagnosis of 21-hydroxylase deficiency
- Parajes, S.
- Quinteiro, C.
- Domínguez, F.
- Loidi, L.
Zeitschrift:
PLoS ONE
ISSN: 1932-6203
Datum der Publikation: 2008
Ausgabe: 3
Nummer: 5
Art: Artikel
