| Autor: |
Cremers, Frans P. M., van de Pol, Dorien J. R., van Driel, Marc, den Hollander, Anneke I., van Haren, Frank J. J., Knoers, Nine V. A. M., Tijmes, Nel, Bergen, Arthur A. B., Rohrschneider, Klaus, Blankenagel, Anita, Pinckers, Alfred J. L. G., Deutman, August F., Hoyng, Carel B. |
| Zdroj: |
Human Molecular Genetics; Mar1998, Vol. 7 Issue 3, p355, 8p |
| Abstrakt: |
Examines the association between splice site mutations in the Stargardt's disease gene and autosomal recessive retinitis pigmentosa and cone-rod dystrophy. Location of lesions in the retina; Inhibitors of the metalloproteinases type 3 gene. |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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