- Title
- Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?
- Creators
- Alejandra Lazaro-Figueroa - Universidad Nacional Autónoma de MéxicoAna Jimena Hernandez-Medrano - Instituto Nacional de Neurología y NeurocirugíaDiana Berenice Ramirez-Pineda - Universidad Nacional Autónoma de MéxicoAndres Navarro Cadavid - Univ Icesi, Lab i2t, CENIT, Cali, ColombiaMary Makarious - National Institute on AgingJia Nee Foo - Nanyang Technological UniversityChelsea X. Alvarado - National Institute of Neurological Disorders and StrokeSara Bandres-Ciga - National Institutes of HealthMaria Teresa Perinan - Hospital Universitario Virgen del RocíoGlobal Parkinsons Genetics Program GP2Karen Nuytemans - UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
- Publication Details
- Movement disorders, Vol.39(11), pp.2117-2119
- Publisher
- Wiley
- Number of pages
- 3
- Grant note
- ZO1 AG000535; ZIA AG000949 / National Institute of Neurological Disorders and Stroke (NINDS); United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Neurological Disorders & Stroke (NINDS) Intramural Research Program of the National Institutes of Health (NIH),National Institute on Aging, NIH, Department of Health and Human Services Aligning Science Across Parkinson's (ASAP) initiative; Aligning Science Across Parkinson's (ASAP) NINDS; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Neurological Disorders & Stroke (NINDS) ASAP initiative MJFF-009421/17483 / The MichaelJ. Fox Foundation; Michael J Fox Foundation National Human Genome Research Institute; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Human Genome Research Institute (NHGRI)
- Academic Unit
- Miller School of Medicine; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation); John P. Hussman Institute for Human Genomics
- Language
- English
- Resource Type
- Journal article
- PMID
- 39133574
- Record Identifier
- 991032796145702976
Journal article
Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?
Movement disorders, Vol.39(11), pp.2117-2119
2024-11-01
PMID: 39133574
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