High frequency of copy number variations and sequence variants at CYP21A2 locus: Implication for the genetic diagnosis of 21-hydroxylase deficiency

1. Parajes, S.
2. Quinteiro, C.
3. Domínguez, F.
4. Loidi, L.

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DOI: 10.1371/JOURNAL.PONE.0002138 GOOGLE SCHOLAR lock_openOpen access editor

Data source: Scopus