Shining a light on CNTNAP2: complex functions to complex disorders
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/ejhg2013100.pdf
Reference74 articles.
1. Nakabayashi K, Scherer SW : The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35. Genomics 2001; 73: 108–112.
2. Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA : CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics 2003; 82: 1–9.
3. Rossi E, Verri AP, Patricelli MG et al: A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea. Eur J Med Genet 2008; 51: 631–638.
4. Poot M, Beyer V, Schwaab I et al: Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. Neurogenetics 2010; 11: 81–89.
5. Friedman JI, Vrijenhoek T, Markx S et al: CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. Mol Psychiatr 2008; 13: 261–266.
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