Newly identified human aminoacyl‐ <scp>tRNA</scp> synthetase complex interacting multifunctional protein 2 ( <scp>AIMP2</scp> ) loss‐of‐function mutations cause neurodevelopmental defects linked to cell death in a zebrafish model

Patrick Mullen, Shenela Lakhani, Joshua Appelbaum, DéJenaé See, Pryce Patterson, Collin M. MacLeod, Alexandra George, Reza Maroofian, Margaret E. Ross, Christopher Francklyn, Alicia M. Ebert

Open source

DOI: 10.1111/febs.70716
Published: 2026-09-10
Container: The FEBS Journal
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1111/febs.70716,
  title = {Newly identified human aminoacyl‐
                    <scp>tRNA</scp>
                    synthetase complex interacting multifunctional protein 2 (
                    <scp>AIMP2</scp>
                    ) loss‐of‐function mutations cause neurodevelopmental defects linked to cell death in a zebrafish model},
  author = {Patrick Mullen and Shenela Lakhani and Joshua Appelbaum and DéJenaé See and Pryce Patterson and Collin M. MacLeod and Alexandra George and Reza Maroofian and Margaret E. Ross and Christopher Francklyn and Alicia M. Ebert},
  year = {2026},
  journal = {The FEBS Journal},
  doi = {10.1111/febs.70716},
  url = {https://doi.org/10.1111/febs.70716}
}

RIS

TY  - JOUR
TI  - Newly identified human aminoacyl‐
                    <scp>tRNA</scp>
                    synthetase complex interacting multifunctional protein 2 (
                    <scp>AIMP2</scp>
                    ) loss‐of‐function mutations cause neurodevelopmental defects linked to cell death in a zebrafish model
AU  - Patrick Mullen
AU  - Shenela Lakhani
AU  - Joshua Appelbaum
AU  - DéJenaé See
AU  - Pryce Patterson
AU  - Collin M. MacLeod
AU  - Alexandra George
AU  - Reza Maroofian
AU  - Margaret E. Ross
AU  - Christopher Francklyn
AU  - Alicia M. Ebert
PY  - 2026
JO  - The FEBS Journal
DO  - 10.1111/febs.70716
UR  - https://doi.org/10.1111/febs.70716
ER  -

APA

Mullen, P., Lakhani, S., Appelbaum, J., See, D., Patterson, P., MacLeod, C. M., George, A., Maroofian, R., Ross, M. E., Francklyn, C., & Ebert, A. M. (2026). Newly identified human aminoacyl‐ <scp>tRNA</scp> synthetase complex interacting multifunctional protein 2 ( <scp>AIMP2</scp> ) loss‐of‐function mutations cause neurodevelopmental defects linked to cell death in a zebrafish model. The FEBS Journal. https://doi.org/10.1111/febs.70716

Source records

crossref · retrieved 2026-09-25T06:32:28.909Z