{
    "PMID": "10090887",
    "TI": "The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.",
    "JT": "American journal of human genetics",
    "BTI": "",
    "DP": "1999-04",
    "AU": "Maugeri A, van Driel M A, van de Pol D J, Klevering B J, van Haren F J, Tijmes N, Bergen A A, Rohrschneider K, Blankenagel A, Pinckers A J, Dahl N, Brunner H G, Deutman A F, Hoyng C B, Cremers F P"
}