High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect

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Veröffentlicht in:	Human mutation 1998, Vol.11 (S1), p.S53-S54
Hauptverfasser:	Polyakov, Alexander Vladimirovich, Dzenis, Irina Genrikhovna, Baharev, Vladimir Anatol'Evich, Evgrafov, Oleg Vadimovich
Format:	Artikel
Sprache:	eng
Schlagworte:	Alternative Splicing - genetics Deoxyribonucleases, Type II Site-Specific - metabolism DNA - genetics DNA - metabolism Family Health Female Founder Effect Gene Frequency Heterozygote Homozygote Humans Introns - genetics Male Mutation Pedigree Point Mutation Russia Steroid 21-Hydroxylase - genetics
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