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SHANK1 Deletions in Males with Autism Spectrum Disorder
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scholarly article
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title
SHANK1 Deletions in Males with Autism Spectrum Disorder
(English)
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main subject
autism spectrum disorder
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autism
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SH3 and multiple ankyrin repeat domains 1
1 reference
stated in
GOA release 2020-03-11
vocalization behavior
1 reference
stated in
GOA release 2020-03-11
author
Mark Lathrop
series ordinal
19
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Lonnie Zwaigenbaum
series ordinal
24
object named as
Lonnie Zwaigenbaum
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Aparna Prasad
object named as
Aparna Prasad
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4
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Dalila Pinto
object named as
Dalila Pinto
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5
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Thomas Bourgeron
object named as
Thomas Bourgeron
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29
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Éric Fombonne
object named as
Eric Fombonne
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23
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Marion Leboyer
object named as
Marion Leboyer
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16
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Richard Delorme
object named as
Richard Delorme
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14
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Christopher Gillberg
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18
object named as
Christopher Gillberg
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Peter Szatmari
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30
object named as
Peter Szatmari
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Evdokia Anagnostou
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21
object named as
Evdokia Anagnostou
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Stephen W. Scherer
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31
object named as
Stephen W Scherer
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Maria Råstam
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17
object named as
Maria Rastam
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Wendy Roberts
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26
object named as
Wendy Roberts
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Jacques L. Michaud
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11
object named as
Jacques L Michaud
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Claire S Leblond
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3
object named as
Claire S Leblond
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Rosanna Weksberg
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22
object named as
Rosanna Weksberg
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Anath C. Lionel
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2
object named as
Anath C Lionel
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Bridget A. Fernandez
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25
object named as
Bridget A Fernandez
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Guillaume Huguet
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15
object named as
Guillaume Huguet
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Gudrun A Rappold
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27
object named as
Gudrun A Rappold
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Christian Marshall
series ordinal
28
object named as
Christian R Marshall
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Irene Drmic
series ordinal
9
object named as
Irene E Drmic
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Ralph Roeth
series ordinal
13
object named as
Ralph Roeth
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Volker Endris
series ordinal
12
object named as
Volker Endris
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author name string
Daisuke Sato
series ordinal
1
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Susan Walker
series ordinal
6
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Irene O'Connor
series ordinal
7
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Carolyn Russell
series ordinal
8
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Fadi F Hamdan
series ordinal
10
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Dimitri J Stavropoulos
series ordinal
20
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language of work or name
English
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publication date
4 May 2012
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published in
American Journal of Human Genetics
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volume
90
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issue
5
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page(s)
879-87
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copyright license
proprietary license
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copyright status
copyrighted
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cites work
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27 September 2017
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27 September 2017
SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism.
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27 September 2017
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27 September 2017
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27 September 2017
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27 September 2017
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27 September 2017
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27 September 2017
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27 September 2017
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29 November 2018
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29 November 2018
Kinesin family member 6 variant Trp719Arg does not associate with angiographically defined coronary artery disease in the Ottawa Heart Genomics Study
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29 November 2018
Novel de novo SHANK3 mutation in autistic patients
1 reference
stated in
PubMed Central
reference URL
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29 November 2018
Combining information from multiple sources in the diagnosis of autism spectrum disorders.
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PubMed Central
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29 November 2018
Identifiers
DOI
10.1016/J.AJHG.2012.03.017
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1955003
Fatcat ID
release_bftsuwdzvvdxnf4fzhmoamest4
1 reference
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Fatcat
reference URL
https://api.fatcat.wiki/v0/release/bftsuwdzvvdxnf4fzhmoamest4
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
OpenCitations bibliographic resource ID
1955003
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1955003
PMC publication ID
3376495
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1955003
PubMed publication ID
22503632
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1955003
ResearchGate publication ID
224037426
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