Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations.

Ross, Owen A

Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations. [electronic resource] - Neurology Jul 2008 - 303; author reply 303-4 p. digital

Publication Type: Letter; Comment

1526-632X

10.1212/01.wnl.0000320511.30222.dd doi


Aphasia, Primary Progressive--genetics
Causality
DNA Mutational Analysis--standards
Genetic Markers--genetics
Genetic Predisposition to Disease--genetics
Genetic Testing--standards
Genetic Variation--genetics
Genotype
Humans
Inheritance Patterns--genetics
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Mutation--genetics
Neurodegenerative Diseases--genetics
Norway
Parkinson Disease--genetics
Protein Serine-Threonine Kinases--genetics
Risk Factors