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The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders.

https://arctichealth.org/en/permalink/ahliterature136693
Source
Parkinsonism Relat Disord. 2011 Jun;17(5):398-9
Publication Type
Article
Date
Jun-2011
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Author
Sara Bech
Anne Nørremølle
Kristian Winge
Lis Hasholt
Niels Tommerup
Kirsten Svenstrup
Jørgen E Nielsen
Lena E Hjermind
Source
Parkinsonism Relat Disord. 2011 Jun;17(5):398-9
Date
Jun-2011
Language
English
Publication Type
Article
Keywords
Adult
Aged
Aged, 80 and over
Cohort Studies
Denmark - epidemiology
Female
Genome-Wide Association Study
Glycine - genetics
Humans
Male
Middle Aged
Mutation - genetics
Neurodegenerative Diseases - classification - genetics
Protein-Serine-Threonine Kinases - genetics
Serine - genetics
PubMed ID
21353620 View in PubMed
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