TY  - GEN
AU  - Schormair,B
AU  - Kemlink,D
AU  - Mollenhauer,B
AU  - Fiala,O
AU  - Machetanz,G
AU  - Roth,J
AU  - Berutti,R
AU  - Strom,T M
AU  - Haslinger,B
AU  - Trenkwalder,C
AU  - Zahorakova,D
AU  - Martasek,P
AU  - Ruzicka,E
AU  - Winkelmann,J
TI  - Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease
SN  - 1399-0004
PY  - 2019///0911
KW  - Adult
KW  - Age of Onset
KW  - Alleles
KW  - DNA Mutational Analysis
KW  - Female
KW  - Genes, Recessive
KW  - Genetic Association Studies
KW  - methods
KW  - Genetic Predisposition to Disease
KW  - Genetic Testing
KW  - Genotype
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation
KW  - Parkinson Disease
KW  - diagnosis
KW  - Pedigree
KW  - Proteins
KW  - genetics
KW  - Risk Factors
KW  - Sequence Analysis, DNA
KW  - Exome Sequencing
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/cge.13124
ER  -