Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders
ORCID
- Julia Baptista: 0000-0003-0915-5028
DOI Link
DOI
10.1038/s41436-021-01222-w
Publication Date
2021-01-01
Publication Title
Genetics in Medicine
Volume
23
Issue
10
ISSN
1098-3600
Embargo Period
9999-12-31
First Page
1912
Last Page
1921
Recommended Citation
May, H., Anyane-Yeboa, K., Jeong, J., Revah-Politi, A., Cohen, J., Chassevent, A., Baptista, J., Baugh, E., Bier, L., Bottani, A., Te, C., Conlon, C., Fluss, J., Guipponi, M., Kim, C., Matsumoto, N., Person, R., Primiano, M., Rankin, J., Shinawi, M., Smith-Hicks, C., Telegrafi, A., Toy, S., Uchiyama, Y., Aggarwal, V., Goldstein, D., & Roche, K. (2021) 'Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders', Genetics in Medicine, 23(10), pp. 1912-1921. Available at: 10.1038/s41436-021-01222-w
This item is under embargo until 31 December 9999
