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69930 Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma
Mauri L; Uebe S; Sticht H; Vossmerbaeumer U; Weisschuh N; Manfredini E; Maselli E; Patrosso M; Weinreb RN; Penco S; Reis A; Pasutto F
Orphanet Journal of Rare Diseases 2016; 11: 108

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