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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Hauptverfasser: Bacchelli, Elena, Ceroni, Fabiola, Pinto, Dalila, Lomartire, Silvia, Giannandrea, Maila, D'Adamo, Patrizia, Bonora, Elena, Parchi, Piero, Tancredi, Raffaella, Battaglia, Agatino, Maestrini, Elena
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2014
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Research
Online Zugang: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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