Associated Papers
Functional studies of novel CYP21A2 mutations detected in Norwegian patients with congenital adrenal hyperplasia.
Brønstad I et al.
Endocrine Connections, 2014
Application of the DHPLC method for mutational detection of the CYP21A2 gene in congenital adrenal hyperplasia.
Tsai LP et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2009
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