K. G. Meilleur

Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease

K. Fischbeck, A. Vortmeyer, F. Mochel, 2009, neurogenetics.

Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19

K. Fischbeck, D. Shriner, C. Blackstone, 2010, neurogenetics.