Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome-Reference-Cited by-同舟云学术

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Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome

Published:2007-03-28 Issue:6 Volume:15 Page:711-713
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Belloso Jose M,Bache Iben,Guitart Miriam,Caballin Maria Rosa,Halgren Christina,Kirchhoff Maria,Ropers Hans-Hilger,Tommerup Niels,Tümer Zeynep

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201824.pdf

Reference11 articles.

1. Rasband MN : It's ‘juxta’ potassium channel!. J Neurosci Res 2004; 76: 749–757.

2. Poliak S, Gollan L, Martinez R et al: Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels. Neuron 1999; 24: 1037–1047.

3. Poliak S, Salomon D, Elhanany H et al: Juxtaparanodal clustering of Shaker-like K− channels in myelinated axons depends on Caspr2 and TAG-1. J Cell Biol 2003; 162: 1149–1160.

4. 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.

5. Strauss KA, Puffenberger EG, Huentelman MJ et al: Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. New Eng J Med 2006; 354: 1370–1377.

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