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See Latest ArticlesProgeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation
American Journal of Medical Genetics, 10/21/09
Madej–Pilarczyk A et al. – Scleroderma–like skin changes in infants, associated with growth retardation and dysmorphic features, suggest premature aging syndrome, requiring genetic testing and counseling of asymptomatic carriers of LMNA mutations.
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Metabolic reprogramming, caloric restriction and aging
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Comparing histopathological classification with MYCN, 1p36 and 17q status detected by fluorescence in situ hybridisation from 14 untreated primary neuroblastomas in Singapore
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