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


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

SUBMITTER: Robinson PN 

PROVIDER: S-EPMC3046476 | biostudies-literature | 2010

REPOSITORIES: biostudies-literature

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