Cargando…
A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia
Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer disease. Five to ten percent of patients have monogenic form of the disease, while most of sporadic PD cases are caused by the combination of genetic and environmental factors. Microtubule-associated p...
Autores principales: | Smaili, Imane, Hajjaj, Imane, Razine, Rachid, Tibar, Houyam, Salmi, Ayyoub, Bouslam, Naima, Moussa, Ahmed, Regragui, Wafa, Bouhouche, Ahmed |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732378/ https://www.ncbi.nlm.nih.gov/pubmed/33343949 http://dx.doi.org/10.1155/2020/8813344 |
Ejemplares similares
-
Evidence for prehistoric origins of the G2019S mutation in the North African Berber population
por: Ben El Haj, Rafiqua, et al.
Publicado: (2017) -
Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing
por: Bouhouche, Ahmed, et al.
Publicado: (2018) -
LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease
por: Bouhouche, Ahmed, et al.
Publicado: (2017) -
Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report
por: Ouchkat, Fatima, et al.
Publicado: (2020) -
Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel
por: Bouhouche, Ahmed, et al.
Publicado: (2017)