Research map: XXYLT1 and Mendelian Retinal Dystrophy

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  28. Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa · Corinne Bareil · 2001 · 124 citations · Cited by this paper
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  30. An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina. · Grant A. Mitchell · 1988 · 107 citations · Cited by this paper
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