Review
doi: 10.1016/0168-9525(89)90138-8.
Genomic imprinting and genetic disorders in man
- PMID: 2692240
- DOI: 10.1016/0168-9525(89)90138-8
Item in Clipboard
Review
Genomic imprinting and genetic disorders in man
Trends Genet.
1989 Oct.
Abstract
In a considerable number of genetic disorders in the human, the phenotypic expression of the disease can depend on maternal or paternal inheritance of the mutation. It is suggested that genomic imprinting, an epigenetic process that marks maternal and paternal chromosomes in mammals, is involved in such parental effects.
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