A De Novo Gain-of-Function Variant of DNM1L Causes Developmental Encephalopathy.
- DOI
- 10.1016/j.ejmg.2026.105106
- Published
- 2026 Sep 23
- Container
- European journal of medical genetics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.ejmg.2026.105106,
title = {A De Novo Gain-of-Function Variant of DNM1L Causes Developmental Encephalopathy.},
author = {Dong S and Chen Y and Yan M and Huang X and Deng Q and Liao J and Zhang K},
year = {2026},
journal = {European journal of medical genetics},
doi = {10.1016/j.ejmg.2026.105106},
url = {https://doi.org/10.1016/j.ejmg.2026.105106}
}RIS
TY - JOUR TI - A De Novo Gain-of-Function Variant of DNM1L Causes Developmental Encephalopathy. AU - Dong S AU - Chen Y AU - Yan M AU - Huang X AU - Deng Q AU - Liao J AU - Zhang K PY - 2026 JO - European journal of medical genetics DO - 10.1016/j.ejmg.2026.105106 UR - https://doi.org/10.1016/j.ejmg.2026.105106 ER -
APA
S, D., Y, C., M, Y., X, H., Q, D., J, L., & K, Z. (2026). A De Novo Gain-of-Function Variant of DNM1L Causes Developmental Encephalopathy.. European journal of medical genetics. https://doi.org/10.1016/j.ejmg.2026.105106
Source records
- pubmed · retrieved 2026-09-25T11:56:20.557Z