CORD5 |
cord blood-derived embryonic-like stem cells |
dkk-3 |
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[cone-rod dystrophy 12] The designation refers to autosomal dominant cone-rod dystrophy, which is characterized by both cone and rod photoreceptor degeneration and are due to missense mutations in the gene encoding CD133 (prominin-1) (Yang Z et al, 2008).
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