| Species |
Homo sapiens |
| Alternate Name(s) |
RL |
| Epilepsy-Associated Disorder(s) |
temporal lobe epilepsy |
| Description |
reelin
|
| Chromosome |
7
|
| Locus |
7q22 |
| Reference(s) |
Becker AJ, Klein H, Baden T, Aigner L, Normann S, Elger CE, Schramm J, Wiestler OD, Blumcke I. Mutational and expression analysis of the reelin pathway components CDK5 and doublecortin in gangliogliomas. Acta Neuropathol (Berl). 2002 Oct;104(4):403-8. Epub 2002 Jun 19.
Haas CA, Dudeck O, Kirsch M, Huszka C, Kann G, Pollak S, Zentner J, Frotscher M. Role for reelin in the development of granule cell dispersion in temporal lobe epilepsy. J Neurosci. 2002 Jul 15;22(14):5797-802.
Kam R, Chen J, Blumcke I, Normann S, Fassunke J, Elger CE, Schramm J, Wiestler OD, Becker AJ. The reelin pathway components disabled-1 and p35 in gangliogliomas--a mutation and expression analysis. Neuropathol Appl Neurobiol. 2004 Jun;30(3):225-32.
Zhang G, Assadi AH, McNeil RS, Beffert U, Wynshaw-Boris A, Herz J, Clark GD, D'Arcangelo G. The Pafah1b Complex Interacts with the Reelin Receptor VLDLR. PLoS ONE. 2007 Feb 28;2:e252.
|
