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High carrier frequency of 21-hydroxylase deficiency in Cyprus

A A P Phedonos1, C Shammas, N Skordis

  • 1Department of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, 1683, Nicosia, Cyprus.

Clinical Genetics
|April 23, 2013
PubMed

Keywords:
21-hydroxylase deficiencyCYP21A2 geneCypruscongenital adrenal hyperplasia

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