Article

p.L1795F LRRK2 variant is a common cause of Parkinson’s disease in Central Europe

2024-05-29

Abstract excerpt

<title>Abstract</title> <p>Pathogenic variants in <italic>LRRK2</italic> are one of the most common genetic risk factors for Parkinson’s disease (PD). Recently, the lesser-known p.L1795F variant was proposed as a strong genetic risk factor for PD, however, further families are currently lacking in literature. A multicentre young onset and familial PD cohort (n = 220) from 9 movement disorder centres across Centra...

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Literature Corpus work: c0e09fe2-74bb-549e-a32d-1d2295585678
DOI: 10.21203/rs.3.rs-4378197/v1

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