Predicting incidences of neurodevelopmental disorders
Author:
Affiliation:
1. Institute of Human Genetics, University of Leipzig Medical Center, 04103 Leipzig, Germany
Abstract
Publisher
Oxford University Press (OUP)
Subject
Clinical Neurology
Link
http://academic.oup.com/brain/article-pdf/143/4/1046/33111063/awaa079.pdf
Reference8 articles.
1. The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009;Bayat;Epilepsia,2015
2. De novo variants in neurodevelopmental disorders with epilepsy;Heyne;Nat Genet,2018
3. A catalogue of new incidence estimates of monogenic neurodevelopmental disorders caused by de novo variants;López-Riviera;Brain,2020
4. GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects;Platzer;J Med Genet,2017
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