Samir Belal

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

M. Pericak-Vance, W. Hung, T. Siddique, 1994, Human molecular genetics.

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

G. Gyapay, J. Weissenbach, D. Le Paslier, 1995, American journal of human genetics.

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families

J. Beckmann, G. Sirugo, M. Koenig, 1993, Neurology.

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus

Y. Agid, G. Stevanin, M. Hamida, 1994, Neurology.

Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria

M. Ben Hamida, F. Hentati, N. Kaabachi, 2004, Acta Neuropathologica.