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Laminopathies

Published:2018-12-17 Issue:1 Volume:9 Page:543-544
ISSN:1949-1034
Container-title:Nucleus
language:en
Short-container-title:Nucleus

Author:

Lattanzi Giovanna¹²,Maggi Lorenzo³,Araujo-Vilar David⁴

Affiliation:

1. CNR Institute of Molecular Genetics, Unit of Bologna, Bologna, Italy

2. Rizzoli Orthopedic Institute, Bologna, Italy

3. Neurology IV - Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico “Carlo Besta”, Milan, Italy

4. UETeM-Molecular Pathology Group. Department of Medicine, IDIS-CIMUS, University of Santiago de Compostela, Spain

Publisher

Informa UK Limited

Subject

Cell Biology

Link

https://tandfonline.com/doi/pdf/10.1080/19491034.2018.1515606

Reference2 articles.

1. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

2. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Cited by 10 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. Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience;Biomedicines;2024-06-11

2. Role of Lamin A/C as Candidate Biomarker of Aggressiveness and Tumorigenicity in Glioblastoma Multiforme;Biomedicines;2021-09-28

3. Laminopathies’ Treatments Systematic Review: A Contribution Towards a ‘Treatabolome’;Journal of Neuromuscular Diseases;2021-05-13

4. Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness;Brain;2021-05-08

5. Case Report: An Atypical Form of Familial Partial Lipodystrophy Type 2 Due to Mutation in the Rod Domain of Lamin A/C;Frontiers in Endocrinology;2021-04-19

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