Associated Papers
Mutation Analysis of DNAJC Family for Early-Onset Parkinson's Disease in a Chinese Cohort.
Li C et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2020
DNAJC13 mutation screening in patients with Parkinson's disease from South Italy.
Gagliardi M et al.
Parkinsonism & Related Disorders, 2018
Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease.
Ross JP et al.
Neurobiology of Aging, 2016
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
25671699 (PubMed )
Supplement: pgen.1004955.s006.xlsx › SNVs
XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
Talukder AK et al.
Plos One, 2015
25905921 (PubMed )
Supplement: pone.0123569.s008.xls › BC1_ERR166303
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06Y-01A.domain
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