Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes-Reference-Cited by-同舟云学术

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Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes

Published:2004-04-01 Issue:4 Volume:41 Page:304-308
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Csoka A B

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 134 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lipodystrophic Laminopathies: From Dunnigan Disease to Progeroid Syndromes;International Journal of Molecular Sciences;2024-08-28

2. The farnesyl transferase inhibitor (FTI) lonafarnib improves nuclear morphology in ZMPSTE24-deficient fibroblasts from patients with the progeroid disorder MAD-B;Nucleus;2023-12-05

3. Age‐associated reduction of nuclear shape dynamics in excitatory neurons of the visual cortex;Aging Cell;2023-07-21

4. A subtype of laminopathies: Generalized lipodystrophy‐associated progeroid syndrome caused by LMNA gene c.29C>T mutation;Journal of Diabetes Investigation;2023-07-13

5. Extracellular Matrix Dynamics as an Emerging yet Understudied Hallmark of Aging and Longevity;Aging and disease;2023

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