American Journal of Medical Genetics · 1982 · 33 citations · 15 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsPopulation GeneticsCrossing OverDisorders Of Sex DevelopmentGenetic DisordersGenetic LinkageMuscular DystrophyDuchenne Muscular Dystrophy InheritanceMolecular Basis Of InheritanceMuscular Dystrophy GeneticsMuscular Dystrophy PathophysiologyMutation Rate DeterminationSex Differences In RecombinationUnequal Crossing OverX-linked Infertility
Abstract In order to explain the high mutation rate in Duchenne muscular dystrophy (DMD), together with the apparent equal incidence of new mutations in sperms and ova, which is unusual when compared with other X‐linked conditions, it is postulated that a significant proportion of new mutations in DMD are caused by unequal crossing over in females at meiosis. If this is true, then there are important consequences for the strategy of research into the molecular basis of DMD.
15
The rate of spontaneous mutation of a human gene
J. B. S. Haldane · Journal of Genetics · 1935 · 524 citations
Triplicated alpha-globin loci in humans.
M. Goossens, A M Dozy, Stephen H. Embury et al. · Proceedings of the National Academy of Sciences · 1980 · 241 citations · Full text