An Interstitial 17q11.2 de novo Deletion Involving the CDK5R1 Gene in a High-Functioning Autistic Patient-Reference-Cited by-同舟云学术

An Interstitial 17q11.2 de novo Deletion Involving the CDK5R1 Gene in a High-Functioning Autistic Patient

Published:2018 Issue:5 Volume:9 Page:247-252
ISSN:1661-8769
Container-title:Molecular Syndromology
language:en
Short-container-title:Mol Syndromol

Author:

Lintas Carla,Sacco Roberto,Tabolacci Claudio,Brogna Claudia,Canali Marco,Picinelli Chiara,Tomaiuolo Pasquale,Castronovo Paola,Baccarin Marco,Persico Antonio M.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Reference17 articles.

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2. Gregg JP, Lit L, Baron CA, Hertz-Picciotto I, Walker W, et al: Gene expression changes in children with autism. Genomics 91:22-9 (2008).

3. GTEx Consortium: The Genotype-Tissue Expression (GTEx) project. Nat Genet 45:580-585 (2013).

4. Gupta A, Sanada K, Miyamoto DT, Rovelstad S, Nadarajah B, et al: Layering defect in p35 deficiency is linked to improper neuronal-glial interaction in radial migration. Nat Neurosci 6:1284-1291 (2003).

5. He X, Ishizeki M, Mita N, Wada S, Araki Y, et al: Cdk5/p35 is required for motor coordination and cerebellar plasticity. J Neurochem 131:53-64 (2014).

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