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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
Koyama, Satomi, Toyoura, Takio, Saisho, Sumitaka, Shimozawa, Kazuhiko, Yata, JunichiVolume:
87
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jcem.87.6.8522
Date:
June, 2002
File:
PDF, 220 KB
english, 2002