A. Webber

De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia

A. Dagher, G. Rouleau, Z. Gan-Or, 2016, Neurology: Genetics.

A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroids

B. Brais, M. Guiot, R. La Piana, 2014, neurogenetics.

Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease.

M. Daly, A. Beggs, C. Niemeyer, 2001, Blood.

A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroids

B. Brais, M. Guiot, R. La Piana, 2014, neurogenetics.