Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: Disease Progression and MSH3[original query] |
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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.
The Lancet. Neurology 2017 Jun . Moss Davina J Hensman, Pardiñas Antonio F, Langbehn Douglas, Lo Kitty, Leavitt Blair R, Roos Raymund, Durr Alexandra, Mead Simon, , , Holmans Peter, Jones Lesley, Tabrizi Sarah |
| MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1. Brain : a journal of neurology 2019 6 142 (7): 1876-86. Flower Michael, Lomeikaite Vilija, Ciosi Marc, Cumming Sarah, Morales Fernando, Lo Kitty, Hensman Moss Davina, Jones Lesley, Holmans Peter, , , Monckton Darren G, Tabrizi Sarah |
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- Page last updated:Sep 18, 2023
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