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Identification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients
Sarar Mohamed, Muddathir H. Hamad and Khaled K. Abu-Amero
Saudi Medical Journal September 2015, 36 (9) 1110-1114; DOI: https://doi.org/10.15537/smj.2015.9.12118
Sarar Mohamed
From the Department of Pediatrics (Mohamed, Hamad), the Ophthalmic Genetics Laboratory, Department Of Ophthalmology (Abu-Amero), College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia
MD, FRCPCHMuddathir H. Hamad
From the Department of Pediatrics (Mohamed, Hamad), the Ophthalmic Genetics Laboratory, Department Of Ophthalmology (Abu-Amero), College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia
MD, ABPKhaled K. Abu-Amero
From the Department of Pediatrics (Mohamed, Hamad), the Ophthalmic Genetics Laboratory, Department Of Ophthalmology (Abu-Amero), College of Medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia
PhD, MSc![Loading Loading](https://smj.org.sa/sites/all/modules/contrib/panels_ajax_tab/images/loading.gif)
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Identification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients
Sarar Mohamed, Muddathir H. Hamad, Khaled K. Abu-Amero
Saudi Medical Journal Sep 2015, 36 (9) 1110-1114; DOI: 10.15537/smj.2015.9.12118
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