Heterozygous Variants in Sptbn1 Cause Intellectual Disability and Autism

AuthID
 P-00T-TT9
21
Author(s)
Rosenfeld, JA
·
Xiao, R
·
Bekheirnia, MR
·
Kanani, F
·
Parker, MJ
·
Koenig, MK
·
van Haeringen, A
·
Ruivenkamp, C
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Almeida, PM
·
[+1]·
Basto, JP
·
Palen, E
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Oetjens, KF
·
Burrage, LC
·
Xia, F
·
Liu, PF
·
Eng, CM
·
Yang, YP
·
Posey, JE
·
Lee, BH
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1
Group Author(s)
Undiagnosed Dis Network
Tipo de Documento
Article in Press
Year published
2021
Publicado
in AMERICAN JOURNAL OF MEDICAL GENETICS PART A, ISSN: 1552-4825
Volume: 185, Número: 7, Páginas: 2037-2045 (9)
Indexing
Wos®
Scopus®
Crossref®11
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 33847457
SCOPUS: 2-s2.0-85104357440
Wos: WOS:000639472700001
Source Identifiers
ISSN: 1552-4825
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All authors
Name Order Nome   Name Order Nome   Name Order Nome
1 Rosenfeld, JA;   2 Xiao, R;   3 Bekheirnia, MR;
4 Kanani, F;   5 Parker, MJ;   6 Koenig, MK;
7 van Haeringen, A;   8 Ruivenkamp, C;   9 Rosmaninho Salgado, J;
10 Almeida, PM;   11 Sa, J;   12 Basto, JP;
13 Palen, E;   14 Oetjens, KF;   15 Burrage, LC;
16 Xia, F;   17 Liu, PF;   18 Eng, CM;
19 Yang, YP;   20 Posey, JE;   21 Lee, BH;

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