Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha 2-chain
Allamand, V, Sunada, Y, Salih, MAM, Straub, V, Ozo, C O, Al-Turaiki, MHS, Akbar, M, Kolo, T, Campbell, K P
Published in Human molecular genetics (01.05.1997)
Published in Human molecular genetics (01.05.1997)
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Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity
Salih, M A, Maisonobe, T, Kabiraj, M, al Rayess, M, al-Turaiki, M H, Akbar, M, Tahan, A, Urtizberea, J A, Grid, D, Hamadouche, T, Guilbot, A, Brice, A, Leguern, E
Published in Neuromuscular disorders : NMD (01.01.2000)
Published in Neuromuscular disorders : NMD (01.01.2000)
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A novel form of familial congenital muscular dystrophy in two adolescents
Salih, M A, Al Rayess, M, Cutshall, S, Urtizberea, J A, Al-Turaiki, M H, Ozo, C O, Straub, V, Akbar, M, Abid, M, Andeejani, A, Campbell, K P
Published in Neuropediatrics (01.12.1998)
Published in Neuropediatrics (01.12.1998)
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