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English
OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24
scientific article published on 10 October 2012
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
title
OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
main subject
oculocutaneous albinism
1 reference
based on heuristic
inferred from title
author name string
T Kausar
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
M A Bhatti
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
M Ali
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
R S Shaikh
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
Z M Ahmed
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
publication date
10 October 2012
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
volume
84
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
page(s)
91-93
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
cites work
RETRACTED: A BLOC-1 mutation screen reveals that PLDN is mutated in Hermansky-Pudlak Syndrome type 9.
1 reference
stated in
COCI
retrieved
30 December 2023
reference URL
https://opencitations.net/index/api/v1/citations/10.1016/J.AJHG.2011.05.009
Identifiers
DOI
10.1111/CGE.12019
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
PubMed ID
23050561
1 reference
stated in
Europe PubMed Central
PubMed ID
23050561
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23050561%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 March 2020
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