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.
Revista:
PLoS ONE
ISSN: 1932-6203
Ano de publicación: 2008
Volume: 3
Número: 5
Tipo: Artigo
