(2017). Nonrecurrent PMP22-RAI1 contiguous gene deletions arise from replication-based mechanisms and result in Smith–Magenis syndrome with evident peripheral neuropathy.
Chicago Style (17th ed.) CitationNonrecurrent PMP22-RAI1 Contiguous Gene Deletions Arise from Replication-based Mechanisms and Result in Smith–Magenis Syndrome with Evident Peripheral Neuropathy. 2017.
MLA (8th ed.) CitationNonrecurrent PMP22-RAI1 Contiguous Gene Deletions Arise from Replication-based Mechanisms and Result in Smith–Magenis Syndrome with Evident Peripheral Neuropathy. 2017.
Warning: These citations may not always be 100% accurate.