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English
A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract
scientific article published on 10 October 2007
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
title
A deletion in DRCTNNB1A associated with hypomyelination and juvenile onset cataract
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
author
Aslihan Tolun
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
author name string
Sibel Aylin Ugur
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
publication date
10 October 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
published in
European Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
volume
16
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
page(s)
261-264
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
cites work
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201935
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotyping for human whole-genome scans: past, present, and future
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201935
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/SJ.EJHG.5201935
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
PubMed publication ID
17928815
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17928815
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17928815%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 January 2020
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