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Genotyping data from one patient with unexplained mental retardation and a deletion in 15q13

ABSTRACT: Recurrent deletions on 15q13.3 have been identified as a predisposition to mental retardation, epilepsy and psychiatric disease. We report compound heterozygous deletions on 15q13.3 in one patients with severe encephalopathy and seizures.

ORGANISM(S): Homo sapiens

PROVIDER: GSE20564 | GEO | 2011/03/05

SECONDARY ACCESSION(S): PRJNA125215

REPOSITORIES: GEO

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Genotyping data from one patient with unexplained mental retardation and a deletion in 15q13

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