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Article

[De novo I172N mutation in a patient with 21-hydroxilase deficiency].

Medicina clinica - 3 Jul 2010

Díez López I, Rodríguez Estevez A, González Molina E, Ezquieta Zubicaray B

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Identifiers

PMID: 19576599
DOI: 10.1016/j.medcli.2009.05.011

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