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English
Myelin genes: getting the dosage right
scientific article published on 01 November 1995
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
title
Myelin genes: getting the dosage right
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
author name string
Scherer SS
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
Chance PF
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
publication date
1 November 1995
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
volume
11
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
page(s)
226-228
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng1195-226
0 references
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Biology and genetics of hereditary motor and sensory neuropathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of Trembler and Trembler-J mouse phenotypes: varying severity of peripheral hypomyelination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary demyelinating neuropathy in the Trembler mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1195-226
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1195-226
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
PubMed ID
7581438
1 reference
stated in
Europe PubMed Central
PubMed ID
7581438
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7581438%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 October 2019
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