Search Results - Catro-Feijoo, Lidia

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    High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect

    High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect by 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

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    ORIGINAL ARTICLE: High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect

    ORIGINAL ARTICLE: High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect by Loidi, Lourdes, Quinteiro, Celsa, Parajes, Silvia, Barreiro, Jesus, Leston, Domingo G, Cabezas-Agricola, Jose M, Sueiro, Aurelio M, Araujo-Vilar, David, Catro-Feijoo, Lidia, Costas, Javier, Pombo, Manuel, Dominguez, Fernando

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