G.P.8.12 Molecular characterization and clinical update on one of the earliest described families with severe childhood autosomal recessive muscular dystrophy (SCARMD)

Journal article

Peer reviewed

M. Salih, J.A. Urtizberea, F. Leturcq, M. Mukhtar, L. Anderson and K. Bushby

Neuromuscular disorders : NMD, Vol.17(9), pp.813-813

2007

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Title: G.P.8.12 Molecular characterization and clinical update on one of the earliest described families with severe childhood autosomal recessive muscular dystrophy (SCARMD)
Creators - without role: M. Salih - Division of Pediatric Neurology, Department of Pediatrics, Riyadh, Saudi Arabia
J.A. Urtizberea - Hôpital Marin de Hendaye
F. Leturcq - Hôpital Cochin
M. Mukhtar - University of Khartoum
L. Anderson - Centre for Life
K. Bushby - Centre for Life
Publication Details: Neuromuscular disorders : NMD, Vol.17(9), pp.813-813
Publisher: Elsevier B.V
Identifiers: 9952848808331
Academic Unit: King Saud University
Language: English
Resource Type: Journal article