Articles with "cgl2 patients" as a keyword



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Accelerated epigenetic aging and DNA methylation alterations in Berardinelli–Seip congenital lipodystrophy

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Published in 2023 at "Human Molecular Genetics"

DOI: 10.1093/hmg/ddad016

Abstract: Abstract Berardinelli–Seip congenital lipodystrophy type 2 (CGL2) is a very rare human genetic disorder with potential significance to the understanding of the pathobiology of aging. CGL2 patients display characteristic progeroid features and suffer from type… read more here.

Keywords: dna; cgl2 patients; methylation alterations; dna methylation ... See more keywords