Associated Papers
Identification of LRRK2 missense variants in the accelerating medicines partnership Parkinson's disease cohort.
Bryant N et al.
Human Molecular Genetics, 2021
Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
Kara E et al.
Brain : a Journal of Neurology, 2016
27217339 (PubMed )
Supplement: aww111_supplementary_data.zip › brain-2015-01890-File008.pdf
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