A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11) (Q28215649)

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M J Allen

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A Carey

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M Papaioannou

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C Chakarova

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M Al-Maghtheh

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N D Ebenezer

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C Willis

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A T Moore

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A C Bird

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D M Hunt

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S S Bhattacharya

Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19

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language of work or name

English

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publication date

August 2001

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published in

Molecular Cell

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volume

8

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issue

2

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page(s)

375-81

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Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.

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RP11 is the second most common locus for dominant retinitis pigmentosa

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