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Article

Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH.

Clinical endocrinology - 1 May 2012

Barbaro Michela, Soardi Fernanda C, de Mello Maricilda Palandi, Wedell Anna, Lajic Svetlana

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Share to Adrenal Hyperplasia, Congenital
Share to Child, Preschool
Share to Infant
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

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Share to Severity of Illness Index

Share to Steroid 21-Hydroxylase

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Identifiers

PMID: 22040027
DOI: 10.1111/j.1365-2265.2011.04275.x

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