Skip Header

You are using a version of browser that may not display all the features of this website. Please consider upgrading your browser.
1 to 4 of 4  Show

Literature citations Results

Citation
Novel parkin mutations detected in patients with early-onset Parkinson's disease.

Italian Parkinson Genetics Network
Bertoli-Avella A.M., Giroud-Benitez J.L., Akyol A., Barbosa E., Schaap O., van der Linde H.C., Martignoni E., Lopiano L., Lamberti P., Fincati E. et al.

Mov. Disord. 20:424-431(2005) · UniProtKB (1) · Mapped (22)

GIGYF2 mutations are not a frequent cause of familial Parkinson's disease.

Italian Parkinson Genetics Network
Di Fonzo A., Fabrizio E., Thomas A., Fincati E., Marconi R., Tinazzi M., Breedveld G.J., Simons E.J., Chien H.F., Ferreira J.J. et al.

Parkinsonism Relat. Disord. 15:703-705(2009) · UniProtKB (1) · Mapped (4)

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.

The Italian Parkinson genetics network
Bonifati V., Rohe C.F., Breedveld G.J., Fabrizio E., De Mari M., Tassorelli C., Tavella A., Marconi R., Nicholl D.J., Chien H.F. et al.

Neurology 65:87-95(2005) · UniProtKB (1)

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

The Italian Parkinson genetics network
Di Fonzo A., Rohe C.F., Ferreira J., Chien H.F., Vacca L., Stocchi F., Guedes L., Fabrizio E., Manfredi M., Vanacore N. et al.

Lancet 365:412-415(2005) · UniProtKB (1) · Mapped (4)

1 to 4 of 4  Show
UniProt is an ELIXIR core data resource
Main funding by: National Institutes of Health

We'd like to inform you that we have updated our Privacy Notice to comply with Europe’s new General Data Protection Regulation (GDPR) that applies since 25 May 2018.

Do not show this banner again