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

10.1093/hmg/6.5.747

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Bibliographic Details
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:	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
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/181143
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Institution:	National University of Singapore

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