(Q41055576)
Statements
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Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita (English)
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N Ekhilevitch
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A Kurolap
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D Oz-Levi
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A Mory
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T Hershkovitz
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G Ast
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H Mandel
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H N Baris
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10 December 2015
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90
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1
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84-89
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Identifiers
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