Leucine-Rich Repeat Kinase 2 Gene-Associated Disease: Redefining Genotype-Phenotype Correlation

BACKGROUND: Leucine-rich repeat kinase 2 (LRRK2) has emerged as the most prevalent genetic cause of Parkinson's disease (PD) among Caucasians. Patients carrying an LRRK2 mutation display significant variability of clinical and pathologic phenotypes across and within affected families. METHODS:...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Wider, Christian, Dickson, Dennis W., Wszolek, Zbigniew K.
Materialtyp: Artigo
Språk:Inglês
Publicerad: S. Karger AG 2010
Ämnen:
Imaging, Biomarkers, Genetics and Diagnostic Markers
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2859237/
https://ncbi.nlm.nih.gov/pubmed/20197701
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000289232
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk