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Khan SN 1

Showing records 1 to 1 | Display all abstracts from Khan SN

23420 Null Mutations in LTBP2 Cause Primary Congenital Glaucoma
Ali M; McKibbin M; Booth A; Parry DA; Jain P; Riazuddin SA; Hejtmancik JF; Khan SN; Firasat S; Shires M
American Journal of Human Genetics 2009; 84: 664-671

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