Elevated Frequency and Allelic Heterogeneity of Congenital Nephrotic Syndrome, Finnish Type, in the Old Order Mennonites

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Bibliographische Detailangaben
Veröffentlicht in:	American journal of human genetics 1999-12, Vol.65 (6), p.1785-1790
Hauptverfasser:	Bolk, Stacey, Puffenberger, Erik G., Hudson, Jim, Morton, D. Holmes, Chakravarti, Aravinda
Format:	Artikel
Sprache:	eng
Schlagworte:	Alleles Child, Preschool Christianity Congenital nephrotic syndrome Deletion(s), mutation Female Finland Frequency Gene Frequency - genetics Genetic drift Genetic Heterogeneity Haplotypes - genetics Humans Incidence Infant Letters to the Editor Linkage Disequilibrium - genetics Male Membrane Proteins Mennonite Mutation - genetics Mutation(s), deletion Nephrin Nephrotic Syndrome - congenital Nephrotic Syndrome - ethnology Nephrotic Syndrome - genetics Pedigree Pennsylvania - epidemiology Populations, Mennonite Proteins - genetics
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