Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

No abstract is available for this paper.

• Publication year

  1991

• Venue

  Nature

• Publication date

  1991-12-12

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/354480A0PMID 1684223
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA.

  1991cited by this paper
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  1991cited by this paper
• Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresis.

  1991cited by this paper
• Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

  1991cited by this paper
• Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site.

  1991cited by this paper
• Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.

  1991cited by this paper
• The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

  1991cited by this paper
• Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.

  1990cited by this paper
• A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

  1990cited by this paper
• Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane.

  1990cited by this paper
• Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds).

  1990cited by this paper
• Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction.

  1989cited by this paper
• An electroretinographic and molecular genetic study of X-linked cone degeneration.

  1989cited by this paper
• Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

  1989cited by this paper
• Some cytological and initial biochemical observations on photoreceptors in retinas of rds mice.

  1983cited by this paper
• Development and degeneration of retina in rds mutant mice: Light microscopy

  1980cited by this paper
• A new H-2-linked mutation, rds, causing retinal degeneration in the mouse.

  1978cited by this paper

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  2016cites this paper
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  2016influential citation
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  2016cites this paper
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  2016cites this paper
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  2016cites this paper
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  2016cites this paper
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  2015cites this paper
• Varying the GARP2-to-RDS Ratio Leads to Defects in Rim Formation and Rod and Cone Function.

  2015cites this paper
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  2015influential citation
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  2015cites this paper
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  2015cites this paper
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  2014cites this paper
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  2012cites this paper
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  2011cites this paper
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  2011cites this paper
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  2011cites this paper
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