Development of a new drug for progeria syndrome; Past, Present and Future
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Peertechz Publications Private Limited
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https://www.peertechzpublications.com/articles/AGGR-5-120.pdf
Reference26 articles.
1. 1. M Eriksson, WT Brown, LB Gordon, MW Glynn, J Singer, L Scott, et al. (2003) Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford Progeria Syndrome. Nature 423: 293-298. Link: https://bit.ly/3dE94oY
2. 2. S Gonzalo, R Kreienkamp, P Askjaer (2007) Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations. Ageing Res Reviews 33: 18-29. Link: https://bit.ly/2Ya8N6w
3. 3. RC Hennekam (2006) Hutchinson-Gilford progeria syndrome: review of the phenotype. Am J Med Gene Part A 140: 2603-2624. Link: https://bit.ly/3cDqil0
4. 4. MA Merideth, LB Gordon, S Clauss, V Sachdev, AC Smith, MB Perry, et al. (2008) Phenotype and course of Hutchinson-Gilford progeria syndrome. N Engl J Med 358: 592-604. Link: https://bit.ly/3dD2AXx
5. 5. JI Rodríguez, P Pérez‐Alonso, R Funes, J Pérez‐Rodríguez (1999) Lethal neonatal Hutchinson‐Gilford progeria syndrome. Am J Med Genet 82: 242-248. Link: https://bit.ly/30pLEjx
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