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t/gene-pink1

PINK1 gene

Discuss publications and research concerning the PINK1 gene.

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Related literature

Biallelic hexose-6-phosphate dehydrogenase variants cause mitochondrial dysfunction underlying Parkinson's disease.
PINK1
An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine.
PINK1
From disease to syndrome: the evolution of Parkinson's as a heterogeneous entity.
PINK1
Small Airway Disease in Pre-COPD and Early COPD: Insights Into the Pulmonary "Silent Zone".
PINK1
Rethinking 'rare' PINK1 Parkinson's disease: A meta-analysis of geographical prevalence, phenotypic diversity, and α-synuclein pathology.
PINK1
The Genetic Architecture of Parkinson's Disease in Morocco: Highlighting a Predominance of Mendelian Genes.
PINK1
In Silico Investigation of Parkin-Activating Mutations Using Simulations and Network Modeling.
PINK1
Advancements in Genetic and Biochemical Insights: Unraveling the Etiopathogenesis of Neurodegeneration in Parkinson's Disease.
PINK1
PINK1-PD: A compound heterozygote of Filipino ancestry and 7 Tesla MRI findings.
PINK1
The genetic architecture of mitochondrial dysfunction in Parkinson's disease.
PINK1

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