Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.

Autor: Ferda Percin E; Molecular Ophthalmic Genetics Laboratory, Surgical Research Center, Department of Surgery, University of Connecticut Health Center, Farmington, Connecticut, USA., Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AM, Kalnins VI, Kocak-Altintas A, Sowden JC, Traboulsi E, Sarfarazi M, McInnes RR

Publikováno v: Nature genetics [Nat Genet] 2000 Aug; Vol. 25 (4), pp. 397-401.