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Article

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

5 Jan 2015

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Fetal and Pediatric Neurological Disorders
Genomic variations and chromosomal abnormalities
RNA Research and Splicing

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25560765
DOI: 10.1007/s00439-014-1522-5

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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5PMID 25560765Read ↗

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