G2019S mutation in the leucine-rich repe
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Laurie J. Ozelius; Tatiana Foroud; Susanne May; Geetha Senthil; Paola Sandroni;
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Article
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2007
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John Wiley and Sons
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English
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๐ 1 views
## Abstract Multiple system atrophy (MSA) is characterized clinically by Parkinsonism, cerebellar dysfunction, and autonomic impairment. Multiple mutations in the __LRRK2__ gene are associated with parkinsonian disorders, and the most common one, the G2019S mutation, has been found in โผ1% of sporad