Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry (Q48881167)
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Current Data About Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry
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(P1476) "Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry" (language: en)
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(P2093) R Herrmann
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V Straub
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K Meyer
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T Kahn
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M Wagner
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T Voit
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(P356) 10.1007/BF02282889
(P698) 8911899