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Title: Lamin a truncation in Hutchinson-Gilford progeria
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Science [0036-8075] De Sandre Giovannoli, A yr:2003


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1. Eriksson, M. "Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome." Nature 423.6937 (2003): 293-298. Link to Full Text for this item Link to SFX for this item
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9. Glynn, Michael W W. "Incomplete processing of mutant lamin A in Hutchinson–Gilford progeria leads to nuclear abnormalities, which are reversed by farnesyltransferase inhibition." Human molecular genetics 14.20 (2005): 2959-2969. Link to SFX for this item
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12. Fong, Loren G H. "Blocking protein farnesyltransferase improves nuclear blebbing in mouse fibroblasts with a targeted Hutchinson-Gilford progeria syndrome mutation." Proceedings of the National Academy of Sciences of the United States of America 102.29 (2005): 10291-10296. Link to Full Text for this item Link to SFX for this item
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14. Armanios, M. "The telomere syndromes." Nature reviews. Genetics 13.10 (2012): 693-704. Link to SFX for this item
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