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)
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| Description | scientific article published on March 1, 2013 |
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author: James C Mullikin Tyler Mark Pierson |
| Publication date | March 1, 2013 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |