| Literature DB >> 11803489 |
R Ayyagari1, K Zhang, A Hutchinson, Z Yu, A Swaroop, L E Kakuk, J M Seddon, P S Bernstein, R A Lewis, J Tammur, Z Yang, Y Li, H Zhang, B M Yashar, J Liu, K Petrukhin, P A Sieving, R Allikmets.
Abstract
Stargardt-like macular degeneration (STGD(3)) and autosomal dominant macular degeneration (adMD) share phenotypic characters with atrophic age-related macular degeneration (AMD). Mutations in a photoreceptor cell-specific factor involved in the elongation of very long chain fatty acids (ELOVL(4)) were shown to be associated with STGD(3), adMD, and pattern dystrophy. We screened 778 patients with AMD and 551 age-matched controls to define the role of sequence variants in the ELOVL(4) gene in age-related macular degeneration. We detected three sequence variants in the non-coding region and eight variants in the coding region. No statistically significant association was observed between sequence variants in the ELOVL(4) gene and susceptibility to AMD. However, for the detection of modest effects of multiple alleles in a complex disease, the analysis of larger cohorts of patients may be required.Entities:
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Year: 2001 PMID： 11803489 DOI： 10.1076/opge.22.4.233.2219
Source DB: PubMed Journal: Ophthalmic Genet ISSN： 1381-6810 Impact factor: 1.803