Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD) von Pierson, Tyler Mark, Markello, Thomas, Accardi, John, Wolfe, Lynne, Adams, David, Sincan, Murat, Tarazi, Noor M, Fajardo, Karin Fuentes, Cherukuri, Praveen F, Bajraktari, Ilda, Meilleur, Katy G, Donkervoort, Sandra, Jain, Mina, Hu, Ying, Lehky, Tanya J, Cruz, Pedro, Mullikin, James C, Bonnemann, Carsten, Gahl, William A, Boerkoel, Cornelius F, Tifft, Cynthia J

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