Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. Issue 6 (30th January 2017)

• Record Type: Journal Article
• Authors: Vivero, M.; Cho, M.T.; Begtrup, A.; Wentzensen, I.M.; Walsh, L.; Payne, K.; Zarate, Y.A.; Bosanko, K.; Schaefer, G.B.; DeBrosse, S.; Pollack, L.; Mason, K.; Retterer, K.; DeWard, S.; Juusola, J.; Chung, W.K.
• Is Part Of: Clinical genetics. Volume 91:Issue 6(2017)
• Page Start: 929
• Page End: 931
• Publication Date: 2017-01-30
• Subjects: CLIFAHDD syndrome -- de novo -- NALCN -- neurodevelopmental disorder -- whole‐exome sequencing; Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.12899
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract :