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See Latest ArticlesMutations in ASCC3L1 on chromosome 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese Family
Investigative Ophthalmology and Visual Science, 09/04/09
Li N et al. – These results provide strong evidence that mutations in ASCC3L1 result in autosomal dominant retinitis pigmentosa in this Chinese family.
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