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. 2008 Aug 8;19(4):596–611. doi: 10.1111/j.1750-3639.2008.00198.x

Figure 8.

Figure 8

Cases with confirmed primary laminin‐α2‐deficient congenital muscular dystrophy. A,E. Laminin‐α2 (MAB1922 antibody to the 80 kDa C‐terminal fragment). B,F.β‐Dystroglycan. C,G.α‐Dystroglycan IIH6. D,H.α‐Dystroglycan sheep polyclonal core. A–D: MDC1A (total absence of laminin‐α2); E–H: MDC1A (partial laminin‐α2 deficiency).