Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans

Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans

Human-imprinting disorders are congenital disorders of growth, development and metabolism, associated with disturbance of parent of origin-specific DNA methylation at imprinted loci across the genome. Some imprinting disorders have higher than expected prevalence of monozygotic twinning, of assisted...

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Main Authors: Docherty, Louise E. (Author), Rezwan, Faisal I. (Author), Poole, Rebecca L. (Author), Turner, Claire L.S (Author), Kivuva, Emma (Author), Maher, Eamonn R. (Author), Smithson, Sarah F. (Author), Hamilton-Shield, Julian P. (Author), Patalan, Michal (Author), Gizewska, Maria (Author), Peregud-Pogorzelski, Jaroslaw (Author), Beygo, Jasmin (Author), Buiting, Karin (Author), Horsthemke, Bernhard (Author), Soellner, Lukas (Author), Begemann, Matthias (Author), Eggermann, Thomas (Author), Baple, Emma (Author), Mansour, Sahar (Author), Temple, I. Karen (Author), Mackay, Deborah J.G (Author)
Format: Article
Language:English
Published: 2015-09-01.
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