ObjectiveThere is controversial evidence that FMR1 premutation or “gray zone” (GZ) allele (small CGG expansion, 45–54 repeats) was associated with Parkinson’s disease (PD). We aimed to explore further the association between FMR1 CGG repeat expansions and PD in a large sample of Chinese origin.MethodsWe included a cohort of 2,362 PD patients and 1,072 controls from the Parkinson’s Disease and Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC) in this study and conducted repeat-primed polymerase chain reaction (RP-PCR) for the size of FMR1 CGG repeat expansions.ResultsTwo PD patients were detected with FMR1 premutation (61 and 56 repeats), and the other eleven PD patients were detected with the GZ allele of...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
Background:LRRK2 variants have been demonstrated to have distinct distributions in different populat...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
Study Objectives: The aim of the study was to investigate the relationship between 22 single nucleot...
disease Objectives: The objective of this study is to clarify the role of (G4C2)n expansions in the ...
Objectives: The objective of this study is to clarify the role of (G4C2)n expansions in the etiology...
peer reviewedOBJECTIVES: The objective of this study is to clarify the role of (G4C2)n expansions in...
Objectives: The objective of this study is to clarify the role of (G(4)C(2))(n) expansions in the et...
BackgroundA recent Taiwanese study reported variants of the ubiquinol-cytochrome c reductase core pr...
BACKGROUND: The first large-scale meta-analysis of published genome-wide association studies (GWAS) ...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
Genome-wide association studies (GWAS) on Parkinson’s disease (PD) have mostly been done in European...
Contains fulltext : 97597.pdf (publisher's version ) (Open Access)A previous genom...
<p>Recently, five novel single nucleotide polymorphisms (SNPs), rs10937625 in STK32B (serine/threoni...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
Background:LRRK2 variants have been demonstrated to have distinct distributions in different populat...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
Study Objectives: The aim of the study was to investigate the relationship between 22 single nucleot...
disease Objectives: The objective of this study is to clarify the role of (G4C2)n expansions in the ...
Objectives: The objective of this study is to clarify the role of (G4C2)n expansions in the etiology...
peer reviewedOBJECTIVES: The objective of this study is to clarify the role of (G4C2)n expansions in...
Objectives: The objective of this study is to clarify the role of (G(4)C(2))(n) expansions in the et...
BackgroundA recent Taiwanese study reported variants of the ubiquinol-cytochrome c reductase core pr...
BACKGROUND: The first large-scale meta-analysis of published genome-wide association studies (GWAS) ...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
Genome-wide association studies (GWAS) on Parkinson’s disease (PD) have mostly been done in European...
Contains fulltext : 97597.pdf (publisher's version ) (Open Access)A previous genom...
<p>Recently, five novel single nucleotide polymorphisms (SNPs), rs10937625 in STK32B (serine/threoni...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...
Background:LRRK2 variants have been demonstrated to have distinct distributions in different populat...
IntroductionParkinson's disease (PD) is a progressive movement disorder caused by a loss of dopamine...