Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q57206738)
Watch
English
Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males
scientific article published in The Lancet
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
main subject
neurodevelopmental disorder
1 reference
based on heuristic
inferred from title
author
Graeme Black
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author name string
J Clayton-Smith
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
P Watson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
S Ramsden
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
language of work or name
English
0 references
publication date
1 September 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
356
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
9232
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
830-832
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
cites work
Rett syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rett syndrome in a boy with a 47,XXY karyotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2800%2902661-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(00)02661-1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed publication ID
11022934
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11022934
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11022934%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 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