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Lost in translation: Traversing the complex path from genomics to therapeutics in Autism Spectrum Disorder

Recent progress in the genomics of non-syndromic autism spectrum disorder (nsASD) highlights rare large-effect heterozygous de novo coding mutations. This distinguishes nsASD from later-onset psychiatric disorders where gene discovery efforts have predominantly yielded common alleles of small effect...

詳細記述

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書誌詳細
出版年:Neuron
主要な著者: Sestan, Nenad, State, Matthew W.
フォーマット: Artigo
言語:Inglês
出版事項: 2018
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6989093/
https://ncbi.nlm.nih.gov/pubmed/30359605
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2018.10.015
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