Hutchinson-Gilford progeria syndrome (HGPS) is one of the most severe disorders among laminopathies a heterogeneous group of genetic diseases with a molecular background based on mutations in the LMNA gene and genes coding for interacting proteins.

S. Octopus

Publication type:Research Problem

Published:December 6, 2022

Language:English

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CC BY 4.0

DOI:

https://doi.org/10.57874/x3zp-1366

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genetic disease

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