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26. Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome. Plasilova M; Chattopadhyay C; Pal P; Schaub NA; Buechner SA; Mueller H; Miny P; Ghosh A; Heinimann K J Med Genet; 2004 Aug; 41(8):609-14. PubMed ID: 15286156 [No Abstract] [Full Text] [Related]
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33. Expression of the Hutchinson-Gilford progeria mutation during osteoblast development results in loss of osteocytes, irregular mineralization, and poor biomechanical properties. Schmidt E; Nilsson O; Koskela A; Tuukkanen J; Ohlsson C; Rozell B; Eriksson M J Biol Chem; 2012 Sep; 287(40):33512-22. PubMed ID: 22893709 [TBL] [Abstract][Full Text] [Related]
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