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A subtype of laminopathies: Generalized lipodystrophy‐associated progeroid syndrome caused by LMNA gene c.29C>T mutation

The term laminopathies refers to a group of congenital diseases characterized by accelerated degeneration of human tissues. Mutations in LMNA, LMNB, ZMPSTE24, and other genes lead to structural and functional abnormalities associated with lamins. One subtype of laminopathy is the generalized lipodys...

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Detalles Bibliográficos
Autores principales: Huang, Shipeng, Zhang, Yan, Zhan, Zuan, Gong, Shuhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512909/
https://www.ncbi.nlm.nih.gov/pubmed/37448194
http://dx.doi.org/10.1111/jdi.14055