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VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variants.
Garnier C, Briki F, Nedelec B, Le Pogamp P, Dogan A, Rioux-Leclercq N, Goude R, Beugnet C, Martin L, Delpech M, Bridoux F, Grateau G, Doucet J, Derreumaux P, Valleix S. Garnier C, et al. Among authors: grateau g. Blood. 2017 Dec 21;130(25):2799-2807. doi: 10.1182/blood-2017-07-796185. Epub 2017 Oct 31. Blood. 2017. PMID: 29089309 Free PMC article.
[Physiopathology of amyloidosis].
Grateau G, Delpech M. Grateau G, et al. Ann Med Interne (Paris). 1995;146(3):147-52. Ann Med Interne (Paris). 1995. PMID: 7653914 Review. French. No abstract available.
[Hereditary amyloidosis].
Grateau G, Delpech M. Grateau G, et al. Ann Med Interne (Paris). 1995;146(3):153-6. Ann Med Interne (Paris). 1995. PMID: 7653915 Review. French. No abstract available.
Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF).
Bernot A, da Silva C, Petit JL, Cruaud C, Caloustian C, Castet V, Ahmed-Arab M, Dross C, Dupont M, Cattan D, Smaoui N, Dodé C, Pêcheux C, Nédelec B, Medaxian J, Rozenbaum M, Rosner I, Delpech M, Grateau G, Demaille J, Weissenbach J, Touitou I. Bernot A, et al. Among authors: grateau g. Hum Mol Genet. 1998 Aug;7(8):1317-25. doi: 10.1093/hmg/7.8.1317. Hum Mol Genet. 1998. PMID: 9668175
Hereditary fevers.
Grateau G, Drenth JP, Delpech M. Grateau G, et al. Curr Opin Rheumatol. 1999 Jan;11(1):75-8. doi: 10.1097/00002281-199901000-00013. Curr Opin Rheumatol. 1999. PMID: 9894634 Review.
Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.
Hamidi Asl L, Liepnieks JJ, Hamidi Asl K, Uemichi T, Moulin G, Desjoyaux E, Loire R, Delpech M, Grateau G, Benson MD. Hamidi Asl L, et al. Among authors: grateau g. Am J Pathol. 1999 Jan;154(1):221-7. doi: 10.1016/S0002-9440(10)65268-6. Am J Pathol. 1999. PMID: 9916936 Free PMC article.
315 results