Autosomal Recessive Spastic Paraplegia Type 78 Associated with a Homozygous Variant in the
ATP13A2
Gene
Mov Disord Clin Pract
.
2022 Jul 12;9(7):997-1002.
doi: 10.1002/mdc3.13508.
eCollection 2022 Oct.
Authors
Hussein Algahtani
1
2
3
,
Bader Shirah
4
,
Salem Alshammari
3
,
Fareeda Alghamdi
3
,
Angham Abdulrhman Abdulkareem
5
,
Muhammad Imran Naseer
5
6
Affiliations
1
Neurology Section, Department of Medicine King Abdulaziz Medical City Jeddah Saudi Arabia.
2
Research Office King Abdullah International Medical Research Center Jeddah Saudi Arabia.
3
College of Medicine King Saud bin Abdulaziz University for Health Sciences Jeddah Saudi Arabia.
4
Department of Neuroscience King Faisal Specialist Hospital & Research Centre Jeddah Saudi Arabia.
5
Center of Excellence in Genomic Medicine Research King Abdulaziz University Jeddah Saudi Arabia.
6
Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences King Abdulaziz University Jeddah Saudi Arabia.
PMID:
36247900
PMCID:
PMC9547136
DOI:
10.1002/mdc3.13508
No abstract available
Keywords:
ATP13A2; Saudi Arabia; autosomal recessive; hereditary spastic paraplegia 78; mutation.