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Genetic analysis of Japanese patients with 21-hydroxylase deficiency: identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21.
J Clin Endocrinol Metab
; 87(6): 2668-73, 2002 Jun.
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| MEDLINE | ID: mdl-12050231
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