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Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chain

✍ Scribed by C.A. Sewry; I. Naom; M. D'Alessandro; L. Sorokin; S. Bruno; L.A. Wilson; V. Dubowitz; F. Muntoni

No coin nor oath required. For personal study only.

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