A novel biallelic nonsense variant in SLC38A3 causing epileptic encephalopathy in an Indian family. Issue 5 (20th December 2022)

Record Type:: Journal Article
Title:: A novel biallelic nonsense variant in SLC38A3 causing epileptic encephalopathy in an Indian family. Issue 5 (20th December 2022)
Main Title:: A novel biallelic nonsense variant in SLC38A3 causing epileptic encephalopathy in an Indian family
Authors:: Alawbathani, Salem
Khan, Suliman
Westenberger, Ana
Beetz, Christian
Lingappa, Lokesh
Abstract:: Abstract :
Is Part Of:: Clinical genetics. Volume 103:Issue 5(2023)
Journal:: Clinical genetics
Issue:: Volume 103:Issue 5(2023)
Issue Display:: Volume 103, Issue 5 (2023)
Year:: 2023
Volume:: 103
Issue:: 5
Issue Sort Value:: 2023-0103-0005-0000
Page Start:: 609
Page End:: 611
Publication Date:: 2022-12-20
Subjects:: Medical genetics -- Periodicals
616.0420
Journal URLs:: http://www.blackwell-synergy.com/loi/cge ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/cge.14271 ↗
Languages:: English
ISSNs:: 0009-9163
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.287000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 26913.xml