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English
P gene mutations associated with oculocutaneous albinism type II (OCA2)
scientific article published on 01 March 2005
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
title
P gene mutations associated with oculocutaneous albinism type II (OCA2)
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
main subject
oculocutaneous albinism
1 reference
based on heuristic
inferred from title
author name string
William S Oetting
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Sarah Savage Garrett
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Marcia Brott
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Richard A King
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
publication date
1 March 2005
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
volume
25
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
page(s)
323
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
Identifiers
DOI
10.1002/HUMU.9318
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
PubMed publication ID
15712365
1 reference
stated in
Europe PubMed Central
PubMed publication ID
15712365
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15712365%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
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