(Q48713560)
Statements
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Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain (English)
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Muntoni F
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Sewry CA
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Naom I
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D'Alessandro M
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Sorokin L
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Bruno S
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Wilson LA
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Dubowitz V
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1 May 1997
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7
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3
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169-175
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