Autosomal recessive retinitis pigmentosa and cone–rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

Author: Blankenagel A.  

Publisher: Oxford University Press

E-ISSN: 0964-6906|7|3|355-362

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.7, Iss.3, 1998-03, pp. : 355-362

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