Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder

Citation
Christensen, M. B., Levy, A. M., Mohammadi, N. A., Niceta, M., Kaiyrzhanov, R., Dentici, M. L., Al Alam, C., Alesi, V., Benoit, V., Bhatia, K. P., Bierhals, T., Boßelmann, C. M., Buratti, J., Callewaert, B., Ceulemans, B., Charles, P., De Wachter, M., Dehghani, M., D’haenens, E., … Tümer, Z. (2022). Biallelic variants in <scp>ZNF142</scp> lead to a syndromic neurodevelopmental disorder. Clinical Genetics, 102(2), 98–109. Portico. https://doi.org/10.1111/cge.14165
DOI:
DOI: 10.1111/cge.14165
Year of publication:
2022
Authors participating in BCBHub:
Paulino Gomez-Puertas