(Q41135059)

27 September 2017

title

Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions (English)

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27 September 2017

Jordan SA

1

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27 September 2017

Farrar GJ

series ordinal

2

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27 September 2017

Kenna P

series ordinal

3

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27 September 2017

Humphries P

series ordinal

4

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27 September 2017

publication date

1 January 1992

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27 September 2017

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27 September 2017

volume

1

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27 September 2017

issue

3

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27 September 2017

page(s)

240-247

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Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds).

27 September 2017

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

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Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

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7 January 2021

Analysis of RAS gene mutations in acute myeloid leukemia by polymerase chain reaction and oligonucleotide probes

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

CLUSTAL: a package for performing multiple sequence alignment on a microcomputer

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

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

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

On Some Principles Governing Molecular Evolution

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Theory for protein mutability and biogenesis

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7 January 2021

At last. A standard electroretinography protocol

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

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https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380010311

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380010311

1 reference

27 September 2017

1 reference