(Q47321636)
Statements
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Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutation (English)
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Koss-Harnes D
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Høyheim B
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Jonkman MF
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de Groot WP
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de Weerdt CJ
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Nikolic B
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Wiche G
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Gedde-Dahl T Jr
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1 January 2004
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84
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2
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124-131
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Identifiers
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