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Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland

✍ Scribed by Levo, Antti; Jääskeläinen, Jarmo; Sistonen, Pertti; Sirén, Marja-Kaisa; Voutilainen, Raimo; Partanen, Jukka


Book ID
110024770
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
166 KB
Volume
7
Category
Article
ISSN
1018-4813

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The frequency of 12 different mutations of the steroid 21-hydroxylase gene (CYP21) was investigated in 129 French patients affected by congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase deficiency. Eighty-nine percent of the CAH chromosomes were characterized. The most frequent mutat