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LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact

Movement Disorders
DOI: 10.1002/mds.28452
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Beetz, C., Westenberger, A., Al-Ali, R., Ameziane, N., Alhashmi, N., Boustany, R. M., … Bauer, P. (2021, April 1). LRRK2 Loss-of-Function Variants in Patients with Rare Diseases: No Evidence for a Phenotypic Impact. Movement Disorders. John Wiley and Sons Inc. https://doi.org/10.1002/mds.28452

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