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                                       Details for article 10 of 21 found articles
 
 
  High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect
 
 
Title: High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect
Author: Loidi, Lourdes
Quinteiro, Celsa
Parajes, Silvia
Barreiro, Jesús
Lestón, Domingo G.
Cabezas-Agrícola, José M.
Sueiro, Aurelio M.
Araujo-Vilar, David
Catro-Feijóo, Lidia
Costas, Javier
Pombo, Manuel
Domínguez, Fernando
Appeared in: Clinical endocrinology
Paging: Volume 64 (2006) nr. 3 pages 330-336
Year: 2006-03
Contents:
Publisher: Blackwell Publishing Ltd, Oxford, UK
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 10 of 21 found articles
 
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