LMNA p.H222P mutation causes contractile dysfunction via impaired mitochondrial calcium uptake in human cardiac laminopathy.

Seguret M, Jouve C, Ruiz-Velasco A, Deshayes L, Guesmia Z, Pereira C, Ragot V, Castelli C, Wahbi K, Fauconnier J, Bonne G, Muchir A, Hulot JS

Open source

DOI: 10.1093/cvr/cvag163
Published: 2026 Sep 24
Container: Cardiovascular research
Publisher: Not recorded
Open access: no

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Cite this work

BibTeX

@article{allodium:10.1093/cvr/cvag163,
  title = {LMNA p.H222P mutation causes contractile dysfunction via impaired mitochondrial calcium uptake in human cardiac laminopathy.},
  author = {Seguret M and Jouve C and Ruiz-Velasco A and Deshayes L and Guesmia Z and Pereira C and Ragot V and Castelli C and Wahbi K and Fauconnier J and Bonne G and Muchir A and Hulot JS},
  year = {2026},
  journal = {Cardiovascular research},
  doi = {10.1093/cvr/cvag163},
  url = {https://doi.org/10.1093/cvr/cvag163}
}

RIS

TY  - JOUR
TI  - LMNA p.H222P mutation causes contractile dysfunction via impaired mitochondrial calcium uptake in human cardiac laminopathy.
AU  - Seguret M
AU  - Jouve C
AU  - Ruiz-Velasco A
AU  - Deshayes L
AU  - Guesmia Z
AU  - Pereira C
AU  - Ragot V
AU  - Castelli C
AU  - Wahbi K
AU  - Fauconnier J
AU  - Bonne G
AU  - Muchir A
AU  - Hulot JS
PY  - 2026
JO  - Cardiovascular research
DO  - 10.1093/cvr/cvag163
UR  - https://doi.org/10.1093/cvr/cvag163
ER  -

APA

M, S., C, J., A, R., L, D., Z, G., C, P., V, R., C, C., K, W., J, F., G, B., A, M., & JS, H. (2026). LMNA p.H222P mutation causes contractile dysfunction via impaired mitochondrial calcium uptake in human cardiac laminopathy.. Cardiovascular research. https://doi.org/10.1093/cvr/cvag163

Source records

pubmed · retrieved 2026-09-26T22:40:02.159Z
europe-pmc · retrieved 2026-09-26T22:40:02.174Z
hal · retrieved 2026-09-26T22:40:02.194Z