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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. [electronic resource] by
- 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
Producer: 20000405
In:
American journal of human genetics vol. 64
Availability: No items available.
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