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25. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607 [TBL] [Abstract][Full Text] [Related]
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