1.
A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)
2.
Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects
Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease