Hereditary Syndromes With Signs of Premature Aging
Author:
Publisher
Deutscher Arzte-Verlag GmbH
Subject
General Medicine
Reference38 articles.
1. Martin GM: Genetic modulation of senescent phenotypes in homo sapiens. Cell 2005; 120: 523–32
2. Lessel D, Wu D, Trujillo C, et al.: Dysfunction of the MDM2/p53 axis is linked to premature aging. J Clin Invest 2017; 127: 3598–608
3. Lessel D, Vaz B, Halder S, et al.: Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features. Nat Genet 2014; 46: 1239–44
4. Schrauwen I, Szelinger S, Siniard AL, et al.: A frame-shift mutation in CAV1 is associated with a severe neonatal progeroid and lipodystrophy syndrome. PLoS One 2015; 10: e0131797
5. Puente XS, Quesada V, Osorio FG, et al.: Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome. Am J Hum Genet 2011; 88: 650–6
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