M. Lazar

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)

M. Brodsky, B. Hart, J. Demer, 2003, Nature Genetics.

Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12.

R. Kucherlapati, D. Ward, R. Kucherlapati, 1995, American journal of human genetics.

The p.P56S mutation in the VAPB gene is not due to a single founder: the first European case

P. Trillenberg, M. Zatz, J. Weis, 2010, Clinical genetics.

Retinal vein occlusion associated with methylenetetrahydrofolate reductase mutation.

A. Loewenstein, A. Eldor, M. Lazar, 1999, Ophthalmology.