Biallelic <i><scp>SCN</scp>10A</i> mutations in neuromuscular disease and epileptic encephalopathyMarios Kambouris, Hatem El‐Shanti, Joshi Stephen et al.|Annals of Clinical and Translational Neurology|2016Cited by 25
Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndromeMarios Kambouris, Hatem El‐Shanti, Rachid C. Maroun et al.|Orphanet Journal of Rare Diseases|2014Cited by 19