Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q33748744)
Watch
English
Genetic basis of the human epilepsies
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Genetic basis of the human epilepsies
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
author name string
Gardiner RM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
publication date
1 September 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
published in
Epilepsy Research
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
volume
36
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
issue
2-3
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
page(s)
91-95
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
cites work
A potassium channel mutation in neonatal human epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of a novel gene underlying batten disease, CLN3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Radicals r'aging
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900043-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0920-1211(99)00043-1
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
PubMed ID
10515157
1 reference
stated in
Europe PubMed Central
PubMed ID
10515157
retrieved
29 July 2017
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