Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders

While genes with an excess of de novo mutations (DNMs) have been identified in children with neurodevelopmental disorders (NDDs), few studies focus on DNM patterns where the sex of affected children is examined separately. We considered ∼8,825 sequenced parent-child trios (n ∼26,475 individuals) and...

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Bibliografske podrobnosti
izdano v:Am J Hum Genet
Main Authors: Turner, Tychele N., Wilfert, Amy B., Bakken, Trygve E., Bernier, Raphael A., Pepper, Micah R., Zhang, Zhancheng, Torene, Rebecca I., Retterer, Kyle, Eichler, Evan E.
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2019
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6904808/
https://ncbi.nlm.nih.gov/pubmed/31785789
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2019.11.003
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