Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain
10.1093/hmg/6.5.747
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2020
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sg-nus-scholar.10635-1811432023-11-01T08:14:42Z Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain Allamand, V Sunada, Y Salih, M.A.M Straub, V Ozo, C.O Al-Turaiki, M.H.S Akbar, M Kolo, T Colognato, H Zhang, X Sorokin, L.M Yurchenco, P.D Tryggvason, K Campbell, K.P DUKE-NUS MEDICAL SCHOOL dystrophin laminin alpha chain article Becker muscular dystrophy case report consanguinity controlled study disease severity female gene deletion human human tissue immunohistochemistry male muscular dystrophy phenotype preschool child priority journal protein domain RNA splicing Iva 10.1093/hmg/6.5.747 Human Molecular Genetics 6 5 747-752 2020-10-27T09:58:51Z 2020-10-27T09:58:51Z 1997 Article Allamand, V, Sunada, Y, Salih, M.A.M, Straub, V, Ozo, C.O, Al-Turaiki, M.H.S, Akbar, M, Kolo, T, Colognato, H, Zhang, X, Sorokin, L.M, Yurchenco, P.D, Tryggvason, K, Campbell, K.P (1997). Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain. Human Molecular Genetics 6 (5) : 747-752. ScholarBank@NUS Repository. https://doi.org/10.1093/hmg/6.5.747 09646906 https://scholarbank.nus.edu.sg/handle/10635/181143 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Oxford University Press Unpaywall 20201031 |
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dystrophin laminin alpha chain article Becker muscular dystrophy case report consanguinity controlled study disease severity female gene deletion human human tissue immunohistochemistry male muscular dystrophy phenotype preschool child priority journal protein domain RNA splicing Iva |
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dystrophin laminin alpha chain article Becker muscular dystrophy case report consanguinity controlled study disease severity female gene deletion human human tissue immunohistochemistry male muscular dystrophy phenotype preschool child priority journal protein domain RNA splicing Iva Allamand, V Sunada, Y Salih, M.A.M Straub, V Ozo, C.O Al-Turaiki, M.H.S Akbar, M Kolo, T Colognato, H Zhang, X Sorokin, L.M Yurchenco, P.D Tryggvason, K Campbell, K.P Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain |
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10.1093/hmg/6.5.747 |
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DUKE-NUS MEDICAL SCHOOL |
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DUKE-NUS MEDICAL SCHOOL Allamand, V Sunada, Y Salih, M.A.M Straub, V Ozo, C.O Al-Turaiki, M.H.S Akbar, M Kolo, T Colognato, H Zhang, X Sorokin, L.M Yurchenco, P.D Tryggvason, K Campbell, K.P |
format |
Article |
author |
Allamand, V Sunada, Y Salih, M.A.M Straub, V Ozo, C.O Al-Turaiki, M.H.S Akbar, M Kolo, T Colognato, H Zhang, X Sorokin, L.M Yurchenco, P.D Tryggvason, K Campbell, K.P |
author_sort |
Allamand, V |
title |
Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain |
title_short |
Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain |
title_full |
Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain |
title_fullStr |
Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain |
title_full_unstemmed |
Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain |
title_sort |
mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain |
publisher |
Oxford University Press |
publishDate |
2020 |
url |
https://scholarbank.nus.edu.sg/handle/10635/181143 |
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