Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?

the Global Parkinson's Genetics Program (GP2)

doi:10.1002/mds.29719

Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?

the Global Parkinson's Genetics Program (GP2)

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	2117-2119
Number of pages	3
Journal	Movement Disorders
Volume	39
Issue number	11
DOIs	https://doi.org/10.1002/mds.29719
State	Published - Nov 2024
Externally published	Yes

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10.1002/mds.29719

Cite this

@article{07fb19d472eb463f85db7ddada23ffa9,

title = "Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?",

author = "{the Global Parkinson's Genetics Program (GP2)} and Alejandra L{\'a}zaro-Figueroa and Hern{\'a}ndez-Medrano, {Ana Jimena} and Ram{\'i}rez-Pineda, {Diana Berenice} and {Navarro Cadavid}, Andr{\'e}s and Mary Makarious and Foo, {Jia Nee} and Alvarado, {Chelsea X.} and Sara Bandres-Ciga and Peri{\~n}an, {Maria Teresa}",

year = "2024",

month = nov,

doi = "10.1002/mds.29719",

language = "Ingl{\'e}s",

volume = "39",

pages = "2117--2119",

journal = "Movement Disorders",

issn = "0885-3185",