Transcriptomics

Dataset Information

4

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. We analysed two independent patients with severe encephalopathy and seizures and found heterozygous deletions on 15q13.3 in both patients.

ORGANISM(S): Homo sapiens  

SUBMITTER: Evelin Schröck   Ute Moog  Michael Bonin  Karl Hackmann 

PROVIDER: E-GEOD-20564 | ArrayExpress | 2011-03-05

SECONDARY ACCESSION(S): GSE20564PRJNA125215

REPOSITORIES: GEO, ArrayExpress

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