Saeed Bohlega

Table 3. [DCAF17 Variants Discussed in This GeneReview].

Saeed Bohlega, Fowzan S. Alkuraya, 2016 .

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

Mohamed Abouelhoda, Yong Xiong, Fowzan S Alkuraya, 2015, Cell reports.

SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

Saeed Bohlega, Fowzan S. Alkuraya, F. Alkuraya, 2014, Neurology.

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Pieter J. de Jong, Saeed Bohlega, Jing Liu, 1998, Nature Genetics.