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Expanding the repertoire of RP genes
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scholarly article
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title
Expanding the repertoire of RP genes
(English)
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author
Edwin M. Stone
object named as
Edwin M Stone
series ordinal
1
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language of work or name
English
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publication date
August 1998
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published in
Nature Genetics
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volume
19
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issue
4
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page(s)
311-313
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exact match
https://scigraph.springernature.com/pub.10.1038/1192
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cites work
Molecular genetics of retinitis pigmentosa
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reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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inferred from DOI database lookup
Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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inferred from DOI database lookup
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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inferred from DOI database lookup
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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On the heredity of retinitis pigmentosa
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reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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inferred from DOI database lookup
Identification and characterization of the tuberous sclerosis gene on chromosome 16
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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inferred from DOI database lookup
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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The impact of L1 retrotransposons on the human genome
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reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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inferred from DOI database lookup
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathway leading to correctly folded beta-tubulin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F1192
retrieved
7 January 2021
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inferred from DOI database lookup
Identifiers
DOI
10.1038/1192
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PubMed ID
9697684
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