Survey of plasma proteins in children with progeria pre-therapy and on-therapy with lonafarnib.
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| Abstract | :  Hutchinson-Gilford progeria syndrome (HGPS) is an ultra-rare, fatal, segmental premature aging syndrome caused by the aberrant lamin A protein, progerin. The protein farnesyltransferase inhibitor, lonafarnib, ameliorates some aspects of cardiovascular and bone disease. | 
| Year of Publication | :  2018 | 
| Journal | :  Pediatric research | 
| Date Published | :  2018 | 
| ISSN Number | :  0031-3998 | 
| URL | :  http://dx.doi.org/10.1038/pr.2018.9 | 
| DOI | :  10.1038/pr.2018.9 | 
| Short Title | :  Pediatr Res | 
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