Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy

Journal article

Peer reviewed

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, Vol.23(12), pp.1478-1482

01/12/2002

PMID: 12518196

Abstract

Biological and medical sciences

Investigative techniques, diagnostic techniques (general aspects)

Medical sciences

Osteoarticular system. Muscles

Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques

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Title: Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy
Creators - without role: Mohammed AL-JUMAH - Neurogenetics Laboratory, King Fahad National Guard, Saudi Arabia
Ramanath Majumdar - Neurogenetics Laboratory, King Fahad National Guard, Saudi Arabia
Saad AL-RAJEH - King Saud University
Enrique CHAVES-CARBALLO - Department of Neurosciences, King Faisal Specialist Hospital & Research Center, Saudi Arabia
Mustafa M Salih - King Saud University
Adnan Awada - Neurology Section, King Fahad National Guard, Saudi Arabia
Saad AL-SHAHWAN - Armed Forces Hospital
Shifa AL-UTHAIM - Neurogenetics Laboratory, King Fahad National Guard, Saudi Arabia
Publication Details: Saudi medical journal, Vol.23(12), pp.1478-1482
Publisher: Saudi Medical Journal
Identifiers: 9951806808331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article