Research ArticleOriginal Article
Open Access
Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy
Mohammed Al-Jumah, Ramanath Majumdar, Saad Al-Rajeh, Enrique Chaves-Carballo, Mustafa M. Salih, Adnan Awada, Saad Al-Shahwan and Shifa Al-Uthaim
Saudi Medical Journal December 2002, 23 (12) 1478-1482;
Mohammed Al-Jumah
Neurogenetics Laboratory, Neurology Section, King Fahad National Guard, Riyadh, Kingdom of Saudi Arabia.
Ramanath Majumdar
Department of Medicine, Mail Code 1143, King Fahad National Guard Hospital, PO Box 22490, Riyadh 11426, Kingdom of Saudi Arabia. Tel. +966 (1) 2520088. Ext. 6663. Fax. +966 (1) 2520040. E-mail: [email protected]
Saad Al-Rajeh
Division of Neurology, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Enrique Chaves-Carballo
Department of Neurosciences, King Faisal Specialist Hospital & Research Center, Riyadh, Kingdom of Saudi Arabia.
Mustafa M. Salih
Department of Pediatrics, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Adnan Awada
Neurology Section, King Fahad National Guard Hospital, Riyadh, Kingdom of Saudi Arabia.
Saad Al-Shahwan
Department of Pediatrics, Armed Forces Hospital, Riyadh, Kingdom of Saudi Arabia.
Shifa Al-Uthaim
Neurogenetics Laboratory, King Fahad National Guard Hospital, Riyadh, Kingdom of Saudi Arabia.
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In this issue
Saudi Medical Journal
Vol. 23, Issue 12
1 Dec 2002
Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy
Mohammed Al-Jumah, Ramanath Majumdar, Saad Al-Rajeh, Enrique Chaves-Carballo, Mustafa M. Salih, Adnan Awada, Saad Al-Shahwan, Shifa Al-Uthaim
Saudi Medical Journal Dec 2002, 23 (12) 1478-1482;
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