Varaico: Literature-Extracted Genetic Variants

Gene:SNCG
Variant:p.E108insFs
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SNCG

NM_003087.3:p.E108insFs

Associated Papers

Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.

Periquet M et al.

American Journal of Human Genetics, 2001

Familial Parkinson's disease. Alpha-synuclein and parkin.

Mizuno Y et al.

Advances in Neurology, 2001

Progress in the clinical and molecular genetics of familial parkinsonism.

Kitada T et al.

Neurogenetics, 2000

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

Abbas N et al.

Human Molecular Genetics, 1999

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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."