eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hutchinson-gilford progeria syndrome |
| Comorbidity | C0033300|progeria |
| Sentences | 2 |
| PubMedID- 20559568 | Ftis also improve the progeria-like phenotypes of mouse models of hgps [22], [23]. |
| PubMedID- 22103522 | Hgps (hutchinson-gilford progeria syndrome) is a severe form of progeria in which patients accumulate progerin, a mutant lamin a protein derived from a splicing variant of the lamin a/c gene (lmna). |
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