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Expression data from young and old healthy humans, as well as HGPS patients

GSE69391 Homo sapiens Expression profiling by array 12 samples Submitted 2015/05/30 Platform GPL570
Summary
HGPS is a rare premature ageing disease, caused by a mutation in the LMNA gene, which activates a cryptic splice site, resulting in the production of a mutant lamin A isoform, called progerin. Sporadic usage of the same cryptic splice site has been observed with normal physiological aging. As it is unknown how HGPS causes premature ageing defects, we set out to determine the gene signature of both young healthy individuals, old healthy individuals, as well as HGPS patients.
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Direct links to NCBI, no account and no request form: the whole study as GSE69391_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 12 samples.

Also filed as BioProject PRJNA285353. Searching any of these in the dataset finder brings you back here.

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