Heterozygous Hmgb1 Loss‐Of‐Function Variants Are Associated with Developmental Delay and Microcephaly

AuthID
P-015-H8Q
28
Author(s)
Uguen, K
·
Krysiak, K
·
Audebert‐Bellanger, S
·
Redon, S
·
Benech, C
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Viora‐Dupont, E
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Tran Mau‐Them, F
·
Rondeau, S
·
Elsharkawi, I
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Granadillo, JL
·
[+1]·
[+7]·
Toutain, A
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Bonneau, D
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Gilbert‐Dussardier, B
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Faivre, L
·
Rio, M
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Le Marechal, C
·
Ferec, C
·
Repnikova, E
·
Cao, Y
Document Type
Article
Year published
2021
Published
in Clinical Genetics, ISSN: 0009-9163
Volume: 100, Issue: 4, Pages: 386-395
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ISSN: 0009-9163
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Name Order Name   Name Order Name   Name Order Name
1 Uguen, K;   2 Krysiak, K;   3 Audebert‐Bellanger, S;
4 Redon, S;   5 Benech, C;   6 Viora‐Dupont, E;
7 Tran Mau‐Them, F;   8 Rondeau, S;   9 Elsharkawi, I;
10 Granadillo, JL;   11 Neidich, J;   12 Soares, CA;
13 Tkachenko, N;   14 M. Amudhavalli, S;   15 Engleman, K;
16 Boland, A;   17 Deleuze, J;   18 Bezieau, S;
19 Odent, S;   20 Toutain, A;   21 Bonneau, D;
22 Gilbert‐Dussardier, B;   23 Faivre, L;   24 Rio, M;
25 Le Marechal, C;   26 Ferec, C;   27 Repnikova, E;
28 Cao, Y;