Cita APA

Pierson, T. M., Markello, T., Accardi, J., Wolfe, L., Adams, D., Sincan, M., . . . Tifft, C. J. (2013). 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).

Chicago Style Citation

Pierson, Tyler Mark, et al. 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). 2013.

Cita MLA

Pierson, Tyler Mark, et al. 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). 2013.