Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.

Sprenger HG, Wani G, Hesseling A, König T, Patron M, MacVicar T, Ahola S, Wai T, Barth E, Rugarli EI, Bergami M, Langer T

Open source

DOI: 10.15252/emmm.201809288
Published: 2019 Jan
Container: EMBO molecular medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.15252/emmm.201809288,
  title = {Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.},
  author = {Sprenger HG and Wani G and Hesseling A and König T and Patron M and MacVicar T and Ahola S and Wai T and Barth E and Rugarli EI and Bergami M and Langer T},
  year = {2019},
  journal = {EMBO molecular medicine},
  doi = {10.15252/emmm.201809288},
  url = {https://doi.org/10.15252/emmm.201809288}
}

RIS

TY  - JOUR
TI  - Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.
AU  - Sprenger HG
AU  - Wani G
AU  - Hesseling A
AU  - König T
AU  - Patron M
AU  - MacVicar T
AU  - Ahola S
AU  - Wai T
AU  - Barth E
AU  - Rugarli EI
AU  - Bergami M
AU  - Langer T
PY  - 2019
JO  - EMBO molecular medicine
DO  - 10.15252/emmm.201809288
UR  - https://doi.org/10.15252/emmm.201809288
ER  -

APA

HG, S., G, W., A, H., T, K., M, P., T, M., S, A., T, W., E, B., EI, R., M, B., & T, L. (2019). Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.. EMBO molecular medicine. https://doi.org/10.15252/emmm.201809288

Source records

pubmed · retrieved 2026-09-26T15:46:45.920Z