Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q28251815)
Watch
English
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy
scientific article
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
title
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
main subject
myoclonic epilepsy
1 reference
based on heuristic
inferred from title
juvenile myoclonic epilepsy
1 reference
based on heuristic
inferred from title
author
Andre Hollis Lagrange
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
author name string
Shaochun Ma
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
Marcia A Blair
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
Bassel Abou-Khalil
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
Christina A Gurnett
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
Peter Hedera
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
language of work or name
English
0 references
publication date
12 July 2006
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
published in
Epilepsy Research
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
volume
71
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
issue
2-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
page(s)
129-134
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
cites work
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
1 reference
stated in
COCI
retrieved
9 February 2024
reference URL
https://opencitations.net/index/api/v1/citations/10.1038/NG1121
Identifiers
DOI
10.1016/J.EPLEPSYRES.2006.06.001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
PubMed publication ID
16839746
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16839746
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839746%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit