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TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
Audo I, Kohl S, Leroy BP, Munier FL, Guillonneau X, Mohand-Saïd S, Bujakowska K, Nandrot EF, Lorenz B, Preising M, Kellner U, Renner AB, Bernd A, Antonio A, Moskova-Doumanova V, Lancelot ME, Poloschek CM, Drumare I, Defoort-Dhellemmes S, Wissinger B, Léveillard T, Hamel CP, Schorderet DF, De Baere E, Berger W, Jacobson SG, Zrenner E, Sahel JA, Bhattacharya SS, Zeitz C. Audo I, et al. Among authors: sahel ja. Am J Hum Genet. 2009 Nov;85(5):720-9. doi: 10.1016/j.ajhg.2009.10.013. Epub 2009 Nov 5. Am J Hum Genet. 2009. PMID: 19896113 Free PMC article.
Rod-cone interactions: developmental and clinical significance.
Mohand-Said S, Hicks D, Léveillard T, Picaud S, Porto F, Sahel JA. Mohand-Said S, et al. Among authors: sahel ja. Prog Retin Eye Res. 2001 Jul;20(4):451-67. doi: 10.1016/s1350-9462(01)00006-4. Prog Retin Eye Res. 2001. PMID: 11390256
The aging of the retina.
Bonnel S, Mohand-Said S, Sahel JA. Bonnel S, et al. Among authors: sahel ja. Exp Gerontol. 2003 Aug;38(8):825-31. doi: 10.1016/s0531-5565(03)00093-7. Exp Gerontol. 2003. PMID: 12915204 Review.
684 results