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English
New mutation of pelizaeus--merzbacher-like disease; a report from iran.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
case report
0 references
title
New mutation of pelizaeus--merzbacher-like disease; a report from iran
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
author
Farzad Ahmadabadi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
Alireza Khatami
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
author name string
Parvaneh Karimzadeh
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
Omid Aryani
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
Massoud Houshmand
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
publication date
15 May 2014
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
published in
Iranian journal of radiology : a quarterly journal published by the Iranian Radiological Society
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
volume
11
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
issue
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
page(s)
e6913
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
cites work
Pelizaeus-Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090646
retrieved
5 July 2018
Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090646
retrieved
5 July 2018
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090646
retrieved
5 July 2018
Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090646
retrieved
5 July 2018
The proteolipid protein gene and myelin disorders in man and animal models
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090646
retrieved
5 July 2018
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4090646
retrieved
29 October 2018
Identifiers
DOI
10.5812/IRANJRADIOL.6913
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
PMC publication ID
4090646
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
PubMed publication ID
25035705
1 reference
stated in
Europe PubMed Central
PMC publication ID
4090646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25035705%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 March 2020
ResearchGate publication ID
262687035
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