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How neutral are synonymous codon mutations?
article published in 1995
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instance of
scholarly article
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title
How neutral are synonymous codon mutations?
(English)
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author
Jacques S Beckmann
object named as
Jacques S. Beckmann
series ordinal
2
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author name string
Isabella Richard
series ordinal
1
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language of work or name
English
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publication date
July 1995
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published in
Nature Genetics
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volume
10
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page(s)
259-259
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issue
3
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exact match
https://scigraph.springernature.com/pub.10.1038/ng0795-259
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cites work
Effect on splicing of a silent FGFR2 mutation in Crouzon syndrome
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https://api.crossref.org/works/10.1038%2FNG0795-259
retrieved
21 January 2018
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
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reference URL
https://api.crossref.org/works/10.1038%2FNG0795-259
retrieved
7 January 2021
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Illegitimate transcription: transcription of any gene in any cell type
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0795-259
retrieved
7 January 2021
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Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0795-259
retrieved
7 January 2021
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RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0795-259
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0795-259
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0795-259
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0795-259
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PubMed ID
7670461
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