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Keywords: CYP21A2 genotype
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Journal Articles

Incidence of Classical 21-Hydroxylase Deficiency and Distribution of CYP21A2 Mutations in Estonia

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Subject Area:
Endocrinology , Women's and Children's Health
Kaur Liivak, Simon Tobi, Helene Schlecht, Vallo Tillmann
Journal: Hormone Research in Paediatrics
Hormone Research (2008) 69 (4): 227–232.
https://doi.org/10.1159/000113023
Published Online: 21 January 2008
.... Congenital adrenal hyperplasia 21-Hydroxylase deficiency Classical 21-OHD, incidence CYP21A2 genotype Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive disorders resulting from the deficiency of one of the five enzymes required for the synthesis of cortisol in the adrenal...
View articletitled, Incidence of Classical 21-Hydroxylase Deficiency and Distribution of CYP21A2 Mutations in Estonia
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