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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Bibliografiset tiedot
Päätekijät: Bacchelli, Elena, Ceroni, Fabiola, Pinto, Dalila, Lomartire, Silvia, Giannandrea, Maila, D'Adamo, Patrizia, Bonora, Elena, Parchi, Piero, Tancredi, Raffaella, Battaglia, Agatino, Maestrini, Elena
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2014
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4104741/
https://ncbi.nlm.nih.gov/pubmed/25050139
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-6-17
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