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Mustafa Salih

Mustafa Salih

King Saud University - Riyadh / Saudi Arabia
Medical and Health Sciences / Pediatric Neurology
AD Scientific Index ID: 410943
جامعة الملك سعود
person_outline Mustafa Salih's MOST POPULAR ARTICLES
1-) Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy Nature genetics 32 (2), 267-272, 2002
2-) Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 Nature genetics 25 (1), 17-19, 2000
3-) Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families Cell reports 10 (2), 148-161, 2015
4-) Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis Science 304 (5676), 1509-1513, 2004
5-) Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2 Nature genetics 40 (1), 32-34, 2008