Clinical and pathological characteristics of patients with leucine-rich repeat kinase-2 mutations. [electronic resource]
- Movement disorders : official journal of the Movement Disorder Society Jan 2009
- 32-9 p. digital
Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1531-8257
10.1002/mds.22096 doi
Aged Amino Acid Sequence Cohort Studies DNA Mutational Analysis Female Genes, Dominant Hippocampus--pathology Humans Inclusion Bodies--chemistry Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Male Middle Aged Molecular Sequence Data Mutation, Missense Neurofibrillary Tangles Parkinson Disease--genetics Parkinsonian Disorders--genetics Phosphorylation Phosphoserine--analysis Point Mutation Protein Processing, Post-Translational Protein Serine-Threonine Kinases--chemistry Sequence Alignment Sequence Homology, Amino Acid Temporal Lobe--pathology alpha-Synuclein--analysis