Identification of Novel Co-Occurring <i>ZNF711</i> and <i>SRCAP</i> Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing.
- DOI
- 10.2147/tacg.s625023
- Published
- 2026-09-11
- Container
- Appl Clin Genet
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.2147/tacg.s625023,
title = {Identification of Novel Co-Occurring \<i\>ZNF711\</i\> and \<i\>SRCAP\</i\> Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing.},
author = {Liu T and Huang M and Dai M and Liang Y and Zhang C and Tan J and Qiao F and Wang Y.},
year = {2026},
journal = {Appl Clin Genet},
doi = {10.2147/tacg.s625023},
url = {https://doi.org/10.2147/tacg.s625023}
}RIS
TY - JOUR TI - Identification of Novel Co-Occurring <i>ZNF711</i> and <i>SRCAP</i> Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing. AU - Liu T AU - Huang M AU - Dai M AU - Liang Y AU - Zhang C AU - Tan J AU - Qiao F AU - Wang Y. PY - 2026 JO - Appl Clin Genet DO - 10.2147/tacg.s625023 UR - https://doi.org/10.2147/tacg.s625023 ER -
APA
T, L., M, H., M, D., Y, L., C, Z., J, T., F, Q., & Y., W. (2026). Identification of Novel Co-Occurring <i>ZNF711</i> and <i>SRCAP</i> Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing.. Appl Clin Genet. https://doi.org/10.2147/tacg.s625023
Source records
- europe-pmc · retrieved 2026-09-25T00:34:50.862Z