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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

✍ Scribed by Alessandra Maugeri; Marc A. van Driel; Dorien J.R. van de Pol; B. Jeroen Klevering; Frank J.J. van Haren; Nel Tijmes; Arthur A.B. Bergen; Klaus Rohrschneider; Anita Blankenagel; Alfred J.L.G. Pinckers; Niklas Dahl; Han G. Brunner; August F. Deutman; Carel B. Hoyng; Frans P.M. Cremers

Book ID: 117852771
Publisher: American Society of Human Genetics
Year: 1999
Tongue: English
Weight: 810 KB
Volume: 64
Category: Article
ISSN: 0002-9297
DOI: 10.1086/302323

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