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The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe.
Maugeri A, Flothmann K, Hemmrich N, Ingvast S, Jorge P, Paloma E, Patel R, Rozet JM, Tammur J, Testa F, Balcells S, Bird AC, Brunner HG, Hoyng CB, Metspalu A, Simonelli F, Allikmets R, Bhattacharya SS, D'Urso M, Gonzàlez-Duarte R, Kaplan J, te Meerman GJ, Santos R, Schwartz M, Van Camp G, Wadelius C, Weber BH, Cremers FP. Maugeri A, et al. Among authors: tammur j. Eur J Hum Genet. 2002 Mar;10(3):197-203. doi: 10.1038/sj.ejhg.5200784. Eur J Hum Genet. 2002. PMID: 11973624
Macular pigment and visual acuity in Stargardt macular dystrophy.
Zhang X, Hargitai J, Tammur J, Hutchinson A, Allikmets R, Chang S, Gouras P. Zhang X, et al. Among authors: tammur j. Graefes Arch Clin Exp Ophthalmol. 2002 Oct;240(10):802-9. doi: 10.1007/s00417-002-0554-z. Epub 2002 Sep 14. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 12397427
Evaluation of the ELOVL4 gene in patients with age-related macular degeneration.
Ayyagari R, Zhang K, Hutchinson A, Yu Z, Swaroop A, Kakuk LE, Seddon JM, Bernstein PS, Lewis RA, Tammur J, Yang Z, Li Y, Zhang H, Yashar BM, Liu J, Petrukhin K, Sieving PA, Allikmets R. Ayyagari R, et al. Among authors: tammur j. Ophthalmic Genet. 2001 Dec;22(4):233-9. doi: 10.1076/opge.22.4.233.2219. Ophthalmic Genet. 2001. PMID: 11803489
Duchenne and Becker muscular dystrophies: an Estonian experience.
Talkop UA, Klaassen T, Piirsoo A, Sander V, Napa A, Essenson E, Tammur J, Talvik T. Talkop UA, et al. Among authors: tammur j. Brain Dev. 1999 Jun;21(4):244-7. doi: 10.1016/s0387-7604(99)00016-9. Brain Dev. 1999. PMID: 10392746