Whole genome sequencing reveals biallelic PLA2G6 mutations in siblings with cerebellar atrophy and cap myopathy. Issue 5 (11th February 2021)

• Record Type: Journal Article
• Authors: McMillan, Hugh J.; Marshall, Aren E.; Venkateswaran, Sunita; Hartley, Taila; Warman‐Chardon, Jodi; Ramani, Arun K.; Marshall, Christian R.; Michaud, Jean; Boycott, Kym M.; Dyment, David A.; Kernohan, Kristin D.
• Is Part Of: Clinical genetics. Volume 99:Issue 5(2021)
• Page Start: 746
• Page End: 748
• Publication Date: 2021-02-11
• Subjects: Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.13935
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract :