Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita
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G. Ast | H. Mandel | D. Oz-Levi | H. Baris | N. Ekhilevitch | A. Kurolap | A. Mory | T. Hershkovitz | D Oz-Levi | N Ekhilevitch | A Kurolap | A Mory | T Hershkovitz | G Ast | H Mandel | H N Baris
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