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22. Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin. Stix B; Leber M; Bingemer P; Gross C; Rüschoff J; Fändrich M; Schorderet DF; Vorwerk CK; Zacharias M; Roessner A; Röcken C Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1133-9. PubMed ID: 15790870 [TBL] [Abstract][Full Text] [Related]
23. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene. Augustin S; Llige D; Andreu A; González A; Genescà J Eur J Clin Invest; 2007 Aug; 37(8):673-8. PubMed ID: 17635579 [TBL] [Abstract][Full Text] [Related]
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25. [Study of the molecular bases of familial amyloidotic polyneuropathy]. Maeda S; Tamaoki T No To Shinkei; 2000 Jan; 52(1):14-24. PubMed ID: 10689686 [No Abstract] [Full Text] [Related]
26. Detection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy. Ando Y; Anan I; Suhr O; Holmgren G; Costa PM BMJ; 1998 May; 316(7143):1500-1. PubMed ID: 9582138 [No Abstract] [Full Text] [Related]
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