(Q39195139)
Statements
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A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews (English)
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Dror Sharon
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Noa Auslender
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Anan H Abbasi
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Hanna J Garzozi
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Eyal Banin
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Tamar Ben-Yosef
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1 December 2007
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48
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12
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5431-5438
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Identifiers
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