Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans (Q24685715)

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English	Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans	scientific article

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scholarly article

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Linkage analysis and comparative mapping of canine progressive rod-cone degeneration (prcd) establishes potential locus homology with retinitis pigmentosa (RP17) in humans (English)

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retinitis pigmentosa

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based on heuristic

inferred from title

object named as

K Ray

2

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Elaine Ostrander

7

object named as

E A Ostrander

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author name string

G M Acland

1

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C S Mellersh

3

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W Gu

4

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A A Langston

5

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J Rine

6

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G D Aguirre

8

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language of work or name

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publication date

17 March 1998

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Proceedings of the National Academy of Sciences of the United States of America

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95

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3048-53

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6

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Structure and characterization of the human tissue inhibitor of metalloproteinases-2 gene

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Retinitis pigmentosa locus on 17q (RP17): fine localization to 17q22 and exclusion of the PDEG and TIMP2 genes

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Shared synteny of human chromosome 17 loci in Canids

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Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa

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An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q

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Canine rod transducin alpha-1: cloning of the cDNA and evaluation of the gene as a candidate for progressive retinal atrophy

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A Linkage Map of the Canine Genome

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Nonallelism of erd and prcd and exclusion of the canine RDS/peripherin gene as a candidate for both retinal degeneration loci.

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A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

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1 reference

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Identifiers

10.1073/PNAS.95.6.3048

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1998PNAS...95.3048A

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