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Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease.

AUTHOR(S): Xi Q, Li L, Traboulsi EI, Wang QK.

TITLE: Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt disease. Mol Vis 2009, 15:638-645.

SOURCE

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