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Bonfante A 1

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61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Pasutto F; Mauri L; Popp B; Sticht H; Ekici A; Piozzi E; Bonfante A; Penco S; Schlötzer-Schrehardt U; Reis A
Gene 2015; 568: 76-80

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