Literature DB >> 10884818

Macular degeneration: the emerging genetics.

R A Lewis1, J R Lupski.   

Abstract

Discovery of the gene responsible for a recessive, early-onset maculopathy has focused attention on a biomolecular pathway in which subtle metabolic flaws become toxic to irreplaceable retinal cells. The pathway's identification points toward specific ways of intervening. Among patients with age-related macular degeneration, carriers of single mutations in the same gene are proving to be remarkably common.

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Year:  2000        PMID: 10884818

Source DB:  PubMed          Journal:  Hosp Pract (1995)        ISSN: 2154-8331


  3 in total

Review 1.  Complete characterization of the human ABC gene family.

Authors:  M Dean; R Allikmets
Journal:  J Bioenerg Biomembr       Date:  2001-12       Impact factor: 2.945

2.  Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy.

Authors:  A Maugeri; B J Klevering; K Rohrschneider; A Blankenagel; H G Brunner; A F Deutman; C B Hoyng; F P Cremers
Journal:  Am J Hum Genet       Date:  2000-08-24       Impact factor: 11.025

3.  Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up.

Authors:  Rita Serra; Matteo Floris; Antonio Pinna; Francesco Boscia; Francesco Cucca; Andrea Angius
Journal:  Mol Vis       Date:  2019-12-02       Impact factor: 2.367

  3 in total

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