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9. 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]
10. Unstable enzymes in erythrocytes of a family with the Hutchinson--Gilford progeria syndrome. Goldstein S; Moerman EJ Prog Clin Biol Res; 1978; 21():217-31. PubMed ID: 662891 [No Abstract] [Full Text] [Related]
17. Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature. Mazereeuw-Hautier J; Wilson LC; Mohammed S; Smallwood D; Shackleton S; Atherton DJ; Harper JI Br J Dermatol; 2007 Jun; 156(6):1308-14. PubMed ID: 17459035 [TBL] [Abstract][Full Text] [Related]
18. New approaches to progeria. Kieran MW; Gordon L; Kleinman M Pediatrics; 2007 Oct; 120(4):834-41. PubMed ID: 17908771 [TBL] [Abstract][Full Text] [Related]