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R. L. Watts All authors

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Publications While At HealthPartners

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Journal Article
  • A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. 
  • The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. 
  • Screening for LRRK2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families. 
  • Association study of Parkin gene polymorphisms with idiopathic Parkinson disease. 
  • Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease. 

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  • R. L. Watts

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