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Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

Arimura, T; Helbling-Leclerc, A; Varnous, S; Niel, F; Lacene, E; Fromes, Y; Toussaint, M; Mura, A M; Keller, D I; Amthor, H; Isnard, R; Malissen, M; Schwartz, K; Bonne, G

Authors

T Arimura

A Helbling-Leclerc

S Varnous

F Niel

E Lacene

Y Fromes

M Toussaint

A M Mura

D I Keller

H Amthor

R Isnard

M Malissen

K Schwartz

G Bonne



Citation

Arimura, T., Helbling-Leclerc, A., Varnous, S., Niel, F., Lacene, E., Fromes, Y., Toussaint, M., Mura, A. M., Keller, D. I., Amthor, H., Isnard, R., Malissen, M., Schwartz, K., & Bonne, G. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies. Human Molecular Genetics, 14(1), 155-169. https://doi.org/10.1093/hmg/ddi017

Journal Article Type Article
Deposit Date Nov 11, 2014
Journal Human Molecular Genetics
Print ISSN 0964-6906
Electronic ISSN 1460-2083
Publisher Oxford University Press
Volume 14
Issue 1
Pages 155-169
DOI https://doi.org/10.1093/hmg/ddi017
Public URL https://rvc-repository.worktribe.com/output/1434710
Additional Information Corporate Creators : Ctr Hosp Gen, Paris, Inserm, Paris, Mediterranee



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