Brain Connectivity Changes in Autosomal Recessive Parkinson Disease: A Model for the Sporadic Form

Biallelic genetic mutations in the Park2 and PINK1 genes are frequent causes of autosomal recessive PD. Carriers of single heterozygous mutations may manifest subtle signs of disease, thus providing a unique model of preclinical PD. One emerging hypothesis suggests that non-motor symptom of PD, such...

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Detalles Bibliográficos
Autores principales: Makovac, Elena, Cercignani, Mara, Serra, Laura, Torso, Mario, Spanò, Barbara, Petrucci, Simona, Ricciardi, Lucia, Ginevrino, Monia, Caltagirone, Carlo, Bentivoglio, Anna Rita, Valente, Enza Maria, Bozzali, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082970/
https://www.ncbi.nlm.nih.gov/pubmed/27788143
http://dx.doi.org/10.1371/journal.pone.0163980

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082970/
https://www.ncbi.nlm.nih.gov/pubmed/27788143
http://dx.doi.org/10.1371/journal.pone.0163980

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