Cargando…
Mitochondrial Function in Gilles de la Tourette Syndrome Patients With and Without Intragenic IMMP2L Deletions
Background: Gilles de la Tourette syndrome (GTS) is a neurodevelopmental condition characterized by motor and vocal tics. The underlying etiology remains largely unknown, and GTS is considered as a complex multifactorial disorder associated with effects of several genes in combination with environme...
Autores principales: | Bjerregaard, Victoria A., Schönewolf-Greulich, Bitten, Juel Rasmussen, Lene, Desler, Claus, Tümer, Zeynep |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105681/ https://www.ncbi.nlm.nih.gov/pubmed/32265818 http://dx.doi.org/10.3389/fneur.2020.00163 |
Ejemplares similares
-
Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome
por: Pagliaroli, Luca, et al.
Publicado: (2020) -
Blocking Tics in Gilles de la Tourette Syndrome
por: Kaczyńska, Justyna, et al.
Publicado: (2021) -
Elevated Expression of SLC6A4 Encoding the Serotonin Transporter (SERT) in Gilles de la Tourette Syndrome
por: Hildonen, Mathis, et al.
Publicado: (2021) -
Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome—Where Are We?
por: Levy, Amanda M., et al.
Publicado: (2021) -
Refractory Gilles de la Tourette Syndrome—Many Pieces That Define the Puzzle
por: Szejko, Natalia, et al.
Publicado: (2020)