Work

Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder

Year: 2023

Type: article

Source: European Journal of Human Genetics

DOI: 10.1038/s41431-023-01348-2

Authors: Esmeralda Villavicencio Gonzalez, Ryan S. Dhindsa

Institutions: Baylor College of Medicine, Texas Children's Hospital

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W4362700345

FWCI: 0.146

Cites: 18

Cited by: 1

Related to: 10