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Published in 2020 at "Genes"
DOI: 10.1111/gbb.12687
Abstract: Increasing evidence links heterozygosity for NRXN1 gene deletions to a clinically wide spectrum of neurodevelopmental, psychiatric, and neurological disorders. However, to date, the neurocognitive and social communication features of children carrying this genomic rearrangement have…
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Keywords:
children carrying;
carrying 2p16;
deletion;
neurobehavioral pattern ... See more keywords