Cargando…
Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome
BACKGROUND: Autism Spectrum Conditions (ASC) are neurodevelopmental conditions characterized by difficulties in communication and social interaction, alongside unusually repetitive behaviours and narrow interests. Asperger Syndrome (AS) is one subgroup of ASC and differs from classic autism in that...
Autores principales: | Di Napoli, Agnese, Warrier, Varun, Baron-Cohen, Simon, Chakrabarti, Bhismadev |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350913/ https://www.ncbi.nlm.nih.gov/pubmed/25745553 http://dx.doi.org/10.1186/s13229-015-0009-0 |
Ejemplares similares
-
Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome
por: Di Napoli, Agnese, et al.
Publicado: (2014) -
Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome
por: Durdiaková, Jaroslava, et al.
Publicado: (2014) -
Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism
por: Warrier, Varun, et al.
Publicado: (2013) -
STX1A and Asperger syndrome: a replication study
por: Durdiaková, Jaroslava, et al.
Publicado: (2014) -
A Pooled Genome-Wide Association Study of Asperger Syndrome
por: Warrier, Varun, et al.
Publicado: (2015)