Early-onset Parkinson’s disease associated with a new parkin mutation in a Spanish family-Reference-Cited by-同舟云学术

Early-onset Parkinson’s disease associated with a new parkin mutation in a Spanish family

Published:2001-11 Issue:1-2 Volume:313 Page:108-110
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Alvarez Victoria,Guisasola Luis M.,Moreira Vanessa G.,Lahoz Carlos H.,Coto Eliecer

Publisher

Elsevier BV

Subject

General Neuroscience

Reference19 articles.

1. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe;Abbas;Hum. Mol. Genet.,1999

2. Point mutations (Thr240Arg and Gln311Stop) in the parkin gene;Hattori;Biochem. Biophys. Res. Commun.,1998

3. Importance of familial Parkinson’s disease and parkinsonism to the understanding of nigral degeration in sporadic Parkinson’s disease;Hattori;J. Neural. Transm.,2000

4. Parkin is associated with actin filaments in neuronal and nonneural cells;Huynh;Ann. Neurol.,2000

5. Does failure of parkin-mediated ubiquitination cause juvenile parkinsonism?;Kahle;Trends Biochem. Sci.,2000

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