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Rudkin A 1

Showing records 1 to 1 | Display all abstracts from Rudkin A

47503 Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
Khan K; Rudkin A; Parry DA; Burdon KP; McKibbin M; Logan CV; Abdelhamed ZIA; Muecke JS; Fernandez-Fuentes N; Laurie KJ
American Journal of Human Genetics 2011; 89: 464-473

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