A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder

BACKGROUND: Autism spectrum disorder (ASD) is a highly heritable, neurodevelopmental condition showing extreme genetic heterogeneity. While it is well established that rare genetic variation, both de novo and inherited, plays an important role in ASD risk, recent studies also support a rare recessiv...

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Detalles Bibliográficos
Autores principales: Bacchelli, Elena, Ceroni, Fabiola, Pinto, Dalila, Lomartire, Silvia, Giannandrea, Maila, D'Adamo, Patrizia, Bonora, Elena, Parchi, Piero, Tancredi, Raffaella, Battaglia, Agatino, Maestrini, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104741/
https://www.ncbi.nlm.nih.gov/pubmed/25050139
http://dx.doi.org/10.1186/1866-1955-6-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4104741/
https://www.ncbi.nlm.nih.gov/pubmed/25050139
http://dx.doi.org/10.1186/1866-1955-6-17

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