Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.

Lesage, Suzanne

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. [electronic resource] - Human molecular genetics May 2010 - 1998-2004 p. digital

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

1460-2083

10.1093/hmg/ddq081 doi


Amino Acid Substitution--genetics
Ethnicity--genetics
Evolution, Molecular
Haplotypes--genetics
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Mutation--genetics
Parkinson Disease--genetics
Protein Serine-Threonine Kinases--genetics