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Results: 1-2 |
Results: 2
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
Authors: Boycott, KM Maybaum, TA Naylor, MJ Weleber, RG Robitaille, J Miyake, Y Bergen, AAB Pierpont, ME Pearce, WG Bech-Hansen, NT
Citation: Km. Boycott et al., A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants, HUM GENET, 108(2), 2001, pp. 91-97
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F
Authors: Boycott, KM Pearce, WG Bech-Hansen, NT
Citation: Km. Boycott et al., Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F, CAN J OPHTH, 35(4), 2000, pp. 204-213
Risultati: 1-2 |