Results 101 to 110 of about 944 (117)
Some of the next articles are maybe not open access.
A novel compound heterozygous EPM2A mutation in a Chinese boy with Lafora disease
Neurological Sciences, 2020Yujiao Fu, Xiaosu Yang, Bo Xiao
exaly
Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease
Epilepsia, 2010Gaëtan Lesca +2 more
exaly
Epm2a suppresses tumor growth in an immunocompromised host by inhibiting Wnt signaling
Cancer Cell, 2006Xincheng Zheng +2 more
exaly
Lafora progressive myoclonus epilepsy mutation database-EPM2A and NHLRC1 (EMP2B) genes
Human Mutation, 2005Leonarda Ianzano +2 more
exaly

