Multilocus methylation defects in imprinting disorders

Multilocus methylation defects in imprinting disorders

Mammals inherit two complete sets of chromosomes, one from the father and one from the mother, and most autosomal genes are expressed from both maternal and paternal alleles. In imprinted genes, the expression of the allele is dependent upon its parental origin. Appropriate regulation of imprinted g...

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Bibliographic Details
Main Authors: Mackay Deborah J.G., Eggermann Thomas, Buiting Karin, Garin Intza, Netchine Irène, Linglart Agnès, de Nanclares Guiomar Perez
Format: Article
Language:English
Published: De Gruyter 2015-03-01
Series:Biomolecular Concepts
Subjects:
angelman syndrome
beckwith-wiedemann syndrome
imprinting disorder
multilocus methylation defect
prader-willis syndrome
pseudohypoparathyroidism type 1b
silver-russell syndrome
temple syndrome
transient neonatal diabetes
wang-kagami-ogata syndrome
Online Access:https://doi.org/10.1515/bmc-2014-0037

Internet

https://doi.org/10.1515/bmc-2014-0037

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