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Published in 2018 at "Neuron"
DOI: 10.1016/j.neuron.2018.09.027
Abstract: An understanding of how heterozygous loss-of-function mutations in autism spectrum disorder (ASD) risk genes, such as TBR1, contribute to ASD remains elusive. Conditional Tbr1 deletion during late mouse gestation in cortical layer 6 neurons (Tbr1layer6…
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Keywords:
tbr1 dosage;
cortical layer;
layer;
neonatal tbr1 ... See more keywords