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Genome Biol. 2010;11(12):144. doi: 10.1186/gb-2010-11-12-144. Epub 2010 Dec 21.

Whole-exome sequencing for finding de novo mutations in sporadic mental retardation.

Author information

1
Institute for Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany. peter.robinson@charite.de

Abstract

Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.

PMID:
21172032
PMCID:
PMC3046476
DOI:
10.1186/gb-2010-11-12-144
[Indexed for MEDLINE]
Free PMC Article
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