Genetic epidemiology of Menkes disease Journal Article


Authors: Horn, N.; Morton, N. E.
Article Title: Genetic epidemiology of Menkes disease
Abstract: Copper incorporation studies were performed on individuals from 58 pedigrees, comprising 140 sibships. As previously reported, there is considerable overlap between heterozygotes and normal homozygotes. Segregation analysis supports recessive inheritance of disease, with residual heritability for 64Cu uptake in cultured cells. The population frequency of sporadic cases is compatible with the 1/3 expected for an X-linked lethal with equal mutation rates in egg and sperm, which implies a mutation rate of 6.7 × 10−6/gamete/generation. The parameters estimated here are likely to provide the best basis for genetic counseling until more reliable carrier tests are performed on a systematic sample from a large, defined population. Copyright © 1986 Wiley-Liss, Inc., A Wiley Company
Keywords: clinical article; mutation; genetic analysis; heredity; gene frequency; heterozygote; pedigree; europe; x chromosome; mutation rate; epidemiology; copper; linkage (genetics); genetic epidemiology; menkes syndrome; etiology; inheritance; genes, recessive; human; brain diseases, metabolic; menkes disease; x linkage; menkes kinky hair syndrome
Journal Title: Genetic Epidemiology
Volume: 3
Issue: 4
ISSN: 0741-0395
Publisher: John Wiley & Sons, Inc.  
Date Published: 1986-01-01
Start Page: 225
End Page: 230
Language: English
DOI: 10.1002/gepi.1370030403
PUBMED: 3744020
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 18 August 2021 -- Source: Scopus
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  1. Newton E. Morton
    18 Morton