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The α‐synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases

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Year: 1998
Type: article
Study design: Observational Study
Source: Annals of Neurology
DOI: 10.1002/ana.410440221
Authors: Jenny Vaughan, Alexandra Durr, Johann Tassin, Benjamin Bereznai, Thomas Gasser, Vincenzo Bonifati, Giuseppe De Michele, Edito Fabrizio, Gianpiero Volpe, O. Bandmann, William G. Johnson, Lawrence I. Golbe, Monique Breteler, Giuseppe Meco, Yves Agid, Alexis Brice, C. David Marsden, Nicholas W. Wood
Institutions: National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, Inserm, Physiopathologie des Comportements, LMU Klinikum, München Klinik, Ludwig-Maximilians-Universität München, Sapienza University of Rome, University of Naples Federico II, University of Medicine and Dentistry of New Jersey, Erasmus MC, Erasmus University Rotterdam
Language: English

Topic: Parkinson's Disease Mechanisms and Treatments
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W1967196887
FWCI: 10.73
Cites: 20
Cited by: 80
Related to: 10
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