Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder.
作者信息
Villavicencio Gonzalez Esmeralda, Dhindsa Ryan S
机构信息
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Jan and Dan Duncan Neurologic Research Institute at Texas Children's Hospital, Houston, TX, USA.
出版信息
Eur J Hum Genet. 2023 Sep;31(9):973-974. doi: 10.1038/s41431-023-01348-2. Epub 2023 Apr 7.
Abstract
摘要
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