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Volume 75, Issue 1 , Pages 1-3 , 1 June 2005

No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families

D.P. McKeane
- Research Center for Genetic Medicine, Children's National Medical Center, Washington, DC 20010, United States
- Department of Genetics, George Washington University, Washington, DC 20052, United States
J. Meyer
- Department of Neuro-Behavioral Genetics, University of Trier, D-54290 Trier, Germany
S.E. Dobrin
- Neurobehavioral Unit, Neurogenomics Program, The Translational Genomics Research Institute, Phoenix, AZ 85004, United States
K.M. Melmed
- Neurobehavioral Unit, Neurogenomics Program, The Translational Genomics Research Institute, Phoenix, AZ 85004, United States
S. Ekawardhani
- Department of Neuro-Behavioral Genetics, University of Trier, D-54290 Trier, Germany
N.A. Tracy
- Research Center for Genetic Medicine, Children's National Medical Center, Washington, DC 20010, United States
K.P. Lesch
- Clinical and Molecular Psychobiology, Department of Psychiatry and Psychotherapy, University of Wuerzburg, D-97080 Wuerzburg, Germany
D.A. Stephan
- Neurobehavioral Unit, Neurogenomics Program, The Translational Genomics Research Institute, Phoenix, AZ 85004, United States
- Corresponding author. Tel.: +1 602 3438727; fax: +1 602 3438844.

Received 20 February 2004 ,Revised 21 July 2004 ,Accepted 26 July 2004.

References

Devaney JM, Donarum EA, Brown KM, Meyer J, Stober G, Lesch KP, et al. No missense mutation of WKL1 in a subgroup of probands with schizophrenia. Mol. Psychiatry. 2002;7(4):419–423
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Shutter JR, Scully S, Fan W, Richards WG, Kitajewski J, Deblandre GA, et al. Dll4, a novel Notch ligand expressed in arterial endothelium. Genes Dev. 2000;14(11):1313–1318
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Stober G, Saar K, Ruschendorf F, Meyer J, Nurnberg G, Jatzke S, et al. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15. Am. J. Hum. Genet. 2000;67(5):1201–1207
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