Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain

10.1093/hmg/6.5.747

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Main Authors: 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
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: Oxford University Press 2020
Subjects:
Iva
Online Access:https://scholarbank.nus.edu.sg/handle/10635/181143
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Institution: National University of Singapore
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spelling 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
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic 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
spellingShingle 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
description 10.1093/hmg/6.5.747
author2 DUKE-NUS MEDICAL SCHOOL
author_facet 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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