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English
Lysosomal dysfunctions associated with mutations at mouse pigment genes
scientific article published on May 1, 1979
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
title
Lysosomal dysfunctions associated with mutations at mouse pigment genes
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
main subject
pigmentation
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
genetics
1 reference
stated in
Crossref
DOI
10.1093/GENETICS/92.1.189
reference URL
https://api.crossref.org/works/10.1093/GENETICS/92.1.189
retrieved
29 November 2022
author name string
E. K. Novak
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
R. T. Swank
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
language of work or name
English
0 references
publication date
1 May 1979
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
number of pages
16
1 reference
based on heuristic
inferred from page(s)
full work available at URL
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/115747/pdf/?tool=EBI
file format
Portable Document Format
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/115747/?tool=EBI
file format
HTML
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
http://intl.genetics.org/cgi/content/abstract/92/1/189
online access status
open access
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
https://europepmc.org/articles/PMC1213941
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
https://europepmc.org/articles/PMC1213941?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A115747
retrieved
29 November 2022
http://academic.oup.com/genetics/article-pdf/92/1/189/34424786/genetics0189.pdf
file format
Portable Document Format
1 reference
stated in
Crossref
DOI
10.1093/GENETICS/92.1.189
reference URL
https://api.crossref.org/works/10.1093/GENETICS/92.1.189
retrieved
29 November 2022
published in
Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
volume
92
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
page(s)
189-204
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
cites work
The Chediak-Higashi Syndrome and the Homologous Trait in Animals
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=1213941
retrieved
5 July 2018
Serotonin Deficiency and Prolonged Bleeding in Beige Mice
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=1213941
retrieved
5 July 2018
Ophthalmologic, biochemical, platelet, and ultrastructural defects in the various types of oculocutaneous albinism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/115747
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary defect in platelet function in rats
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/115747
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/GENETICS/92.1.189
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
115747
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=115747
retrieved
29 November 2022
PMCID
1213941
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
PubMed ID
115747
1 reference
stated in
Europe PubMed Central
PubMed ID
115747
retrieved
30 July 2017
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