Author:
Stone Edwin M.,Mathers William D.,Rosenwasser George O.D.,Holland Edward J.,Folberg Robert,Krachmer Jay H.,Nichols Brian E.,Gorevic Peter D.,Taylor Chris M.,Streb Luan M.,Fishbaugh Jill A.,Daley Thomas E.,Sucheski Brian M.,Sheffield Val C.
Publisher
Springer Science and Business Media LLC
Reference32 articles.
1. Midura, R.J. et al. Proteoglycan biosynthesis by human corneas from patients with types 1 and 2 macular corneal dystrophy. J. biol. Chem. 265, 15947–15955 (1990).
2. Meretoja, J. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. Ann. din. Res. 1, 314–324 (1959).
3. de la Chapelle, A. et al. Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187. Nature Genet. 2, 157–160 (1992).
4. Jones, S.T. & Zimmerman, L.E. Histopathologic differentiation of granular, macular and lattice dystrophies of the cornea. Am. J. Ophthal. 51, 394–410 (1961).
5. Folberg, R. et al. Clinically atypical granular corneal dystrophy with pathologic features of lattice-like amyloid deposits: A study of three families. Ophthalmology 95, 46–51 (1988).
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