(Q37613086)
Statements
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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). (English)
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James C Mullikin
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Tyler Mark Pierson
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Thomas Markello
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John Accardi
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Lynne Wolfe
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David Adams
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Murat Sincan
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Noor M Tarazi
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Karin Fuentes Fajardo
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Praveen F Cherukuri
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Ilda Bajraktari
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Katy G Meilleur
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Sandra Donkervoort
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Mina Jain
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Ying Hu
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Tanya J Lehky
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Pedro Cruz
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Carsten Bonnemann
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William A Gahl
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Cornelius F Boerkoel
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Cynthia J Tifft
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Identifiers
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