Citations for
1EIEE28, WWOX
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation.
Mignot C, Lambert L, Pasquier L, Bienvenu T, Delahaye-Duriez A, Keren B, Lefranc J, Saunier A, Allou L, Roth V, Valduga M, Moustaïne A, Auvin S, Barrey C, Chantot-Bastaraud S, Lebrun N, Moutard ML, Nougues MC, Vermersch AI, Héron B, Pipiras E, Héron D, Olivier-Faivre L, Guéant JL, Jonveaux P, Philippe C.
J Med Genet 52(1):61-70. doi: 10.1136/jmedgenet-2014-102748. Epub 2014 Nov 19. 2015
2EIEE28, WWOX
WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period.
Valduga M, Philippe C, Lambert L, Bach-Segura P, Schmitt E, Masutti JP, François B, Pinaud P, Vibert M, Jonveaux P.
J Hum Genet Hum Genet. 2015 M 2015
3EIEE28, WWOX
A spontaneous mutation of the Wwox gene and audiogenic seizures in rats with lethal dwarfism and epilepsy.
Suzuki H, Katayama K, Takenaka M, Amakasu K, Saito K, Suzuki K.
Genes Brain Behav 8(7):650-60. doi: 10.1111/j.1601-183X.2009.00502.x. Epub 2009 May 20. 2009