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PMID: 21076407 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A de novo paradigm for mental retardation.

Nature genetics ·Vol. 42 ·No. 12 ·2010-12-00 ·Pages 1109-12

Vissers LE, de Ligt J, Gilissen C, Janssen I, Steehouwer M, de Vries P, van Lier B, Arts P, Wieskamp N, del Rosario M, van Bon BW, Hoischen A, de Vries BB, Brunner HG, Veltman JA

Abstract

The per-generation mutation rate in humans is high. De novo mutations may compensate for allele loss due to severely reduced fecundity in common neurodevelopmental and psychiatric diseases, explaining a major paradox in evolutionary genetic theory. Here we used a family based exome sequencing approach to test this de novo mutation hypothesis in ten individuals with unexplained mental retardation. We identified and validated unique non-synonymous de novo mutations in nine genes. Six of these, identified in six different individuals, are likely to be pathogenic based on gene function, evolutionary conservation and mutation impact. Our findings provide strong experimental support for a de novo paradigm for mental retardation. Together with de novo copy number variation, de novo point mutations of large effect could explain the majority of all mental retardation cases in the population.

MeSH Terms
Base Sequence Exons/genetics Female Humans Intellectual Disability/genetics Male Mutation/genetics Sequence Analysis, DNA
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Vissers Lisenka E L M
Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences and Institute for Genetic and Metabolic Disorders, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
de Ligt Joep
Gilissen Christian
Janssen Irene
Steehouwer Marloes
de Vries Petra
van Lier Bart
Arts Peer
Wieskamp Nienke
del Rosario Marisol
van Bon Bregje W M
Hoischen Alexander
de Vries Bert B A
Brunner Han G
Veltman Joris A
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Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1546-1718
Published
2010-12-00
Epub
2010-00-14
Pages
1109-12
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Corrections
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