J. E. Young

MEIS1 p.R272H IN FAMILIAL RESTLESS LEGS SYNDROME

M. Farrer, H. Chai, R. Uitti, 2009, Neurology.

Susceptibility genes for restless legs syndrome are not associated with Parkinson disease

M. Farrer, R. Uitti, Z. Wszolek, 2008, Neurology.

11-cis retinol dehydrogenase mutations as a major cause of the congenital night-blindness disorder known as fundus albipunctatus.

D. Han, F. Gonzalez-fernandez, S. Newman, 1999, Molecular vision.

Specific caspase interactions and amplification are involved in selective neuronal vulnerability in Huntington's disease

A. Hackam, M. Hayden, B. Leavitt, 2004, Cell Death and Differentiation.