Autor/a

Clarimón, Jordi

Kulisevsky, Jaime

Universitat Autònoma de Barcelona

Fecha de publicación

2013

Resumen

Breakthroughs in genetics over the last decade have radically advanced our understanding of the etiological basis of Parkinson's disease (PD). Although much research remains to be done, the main genetic causes of this neurodegenerative disorder are now partially unraveled, allowing us to feel more confident that our knowledge about the genetic architecture of PD will continue to increase exponentially. How and when these discoveries will be introduced into general clinical practice, however, remains uncertain. In this review, we provide a general summary of the progress in the genetics of PD and discuss how this knowledge will contribute to the diagnosis and clinical management of patients with, or at risk of this disorder.

Tipo de documento

Article

Lengua

Inglés

Materias y palabras clave

Genetics; Parkinson's disease; Mendelian genes; Genetic testing; PARK; Clinical genetics; Genetic risk factor

Publicado por

 

Documentos relacionados

Current Genomics ; Vol. 14 (december 2013), p. 560-567

Derechos

open access

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https://creativecommons.org/licenses/by-nc/4.0/

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