Varaico: Literature-Extracted Genetic Variants

Gene:PRKN
Variant:p.G77A
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PRKN

NM_004562.3:p.G77A

Associated Papers

An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine.

Asmi S et al.

Ageing Research Reviews, 2026

Saturation genome editing maps the functional spectrum of pathogenic VHL alleles.

Buckley M et al.

Nature Genetics, 2024

38969834 (PubMed )
Supplement: 41588_2024_1800_MOESM4_ESM.xlsx › ST1

Investigation of USP30 inhibition to enhance Parkin-mediated mitophagy: tools and approaches.

Tsefou E et al.

The Biochemical Journal, 2021

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