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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Dades bibliogràfiques
Publicat a:PLoS One
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2016
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5082970/
https://ncbi.nlm.nih.gov/pubmed/27788143
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0163980
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