LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.

Gaig, Carles

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance. [electronic resource] - Archives of neurology Mar 2006 - 377-82 p. digital

Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't

0003-9942

10.1001/archneur.63.3.377 doi


Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Arginine--genetics
Child
Child, Preschool
DNA Mutational Analysis
Family Health
Female
Gene Frequency
Genetic Predisposition to Disease
Glycine--genetics
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Male
Middle Aged
Mutation
Parkinson Disease--epidemiology
Pedigree
Protein Serine-Threonine Kinases--genetics
Serine--genetics
Spain--epidemiology