Zhou, X., Feliciano, P., Shu, C., Wang, T., Astrovskaya, I., Hall, J. B., Obiajulu, J. U., Wright, J. R., Murali, S. C., Xu, S. X., Brueggeman, L., Thomas, T. R., Marchenko, O., Fleisch, C., Barns, S. D., Snyder, L. G., Han, B., Chang, T. S., Turner, T. N., … Chung, W. K. (2022). Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes. Nature Genetics, 54(9), 1305–1319. https://doi.org/10.1038/s41588-022-01148-2
Subjects:
Autism Spectrum Disorders
(OpenAlex Topic)
Molecular Basis of Rett Syndrome and Related Disorders
(OpenAlex Topic)
Standards and Guidelines for Genetic Variant Interpretation
(OpenAlex Topic)
Autism Spectrum Disorder
(MeSH)
Autistic Disorder
(MeSH)
Publication Type:
Article
Unique ID:
10.1038/s41588-022-01148-2
PMID:
Journal:
Publication Date:
Data Source:
PubMed