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

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

Abstract 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 generalize...

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Bibliographic Details
Main Authors: Shipeng Huang, Yan Zhang, Zuan Zhan, Shuhao Gong
Format: Article
Language:English
Published: Wiley 2023-10-01
Series:Journal of Diabetes Investigation
Subjects:
Congenital Generalized
Diabetes Mellitus
Laminopathies
Lipoatrophic
Lipodystrophy
Progeria Syndrome
Online Access:https://doi.org/10.1111/jdi.14055

Internet

https://doi.org/10.1111/jdi.14055

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