LRRK2 gene G2019S mutation and SNPs [haplotypes] in subtypes of Parkinson's disease

Keyphrases

• Age of Onset 20%
• Allele Distribution 10%
• Allele Frequency 10%
• Association Analysis 10%
• Autosomal Recessive Parkinsonism 10%
• Correction for multiple Comparison 10%
• Disease Groups 20%
• Familial PD 30%
• Family History 10%
• First-degree Relatives 10%
• G2019S mutation 100%
• Genotype Distribution 10%
• Genotype Frequency 10%
• Idiopathic Parkinson's Disease 40%
• Leucine-rich Repeat Kinase 2 (LRRK2) 100%
• Non-Hispanic White 10%
• Parkinson Patients 10%
• Parkinson's Disease 100%
• Risk Factors 10%
• Same-race 10%
• Small Fraction 10%
• SNP 30%
• SNP Alleles 10%
• SNP Genotyping 10%
• SNP Haplotype 100%
• Sporadic PD 30%
• White Population 20%

Biochemistry, Genetics and Molecular Biology

• Allele 60%
• Autosomal Dominant Inheritance 20%
• Genotyping 60%
• Haplotype 100%
• Kinase 100%
• Leucine-Rich Repeat 100%
• Phosphotransferase 100%
• Single Nucleotide Polymorphism 100%

Neuroscience

• Familial Parkinson's Disease 25%
• Haplotype 100%
• Leucine Rich Repeat Kinase 2 100%
• Parkinson's Disease 100%