Varaico: Literature-Extracted Genetic Variants

Gene:PRKN
Variant:p.R156_V157insT
Back to variants list

PRKN

NM_004562.3:p.R156_V157insT

Associated Papers

Assessing mutant p53 in primary high-grade serous ovarian cancer using immunohistochemistry and massively parallel sequencing.

Cole AJ et al.

Scientific Reports, 2016

27189670 (PubMed )
Supplement: srep26191-s1.pdf

Biomarkers in Parkinson Disease: global gene expression analysis in peripheral blood from patients with and without mutations in PARK2 and PARK8.

Aguiar PM et al.

Einstein (sao Paulo, Brazil), 2010

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.

Nuytemans K et al.

Human Mutation, 2010

20506312 (PubMed )
Supplement: humu0031-0763-SD1.pdf

Clinical and molecular neuroimaging characteristics of Brazilian patients with Parkinson's disease and mutations in PARK2 or PARK8 genes.

Barsottini OG et al.

Arquivos De Neuro-psiquiatria, 2009

Genetic and environmental findings in early-onset Parkinson's disease Brazilian patients.

Aguiar Pde C et al.

Movement Disorders : Official Journal of the Movement Disorder Society, 2008

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."