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Volume 58, Issue 3
De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features
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Neurogenetics
Original research
De novo variants in
SIAH1,
encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features
Online download statistics by month:
Online download statistics by month: May 2020 to August 2023
Abstract
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Pdf
May 2020
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Jun 2020
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Jul 2020
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Aug 2020
195
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Sep 2020
73
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Oct 2020
92
8
8
Nov 2020
116
3
2
Dec 2020
164
16
6
Jan 2021
63
4
5
Feb 2021
421
29
23
Mar 2021
324
26
18
Apr 2021
339
19
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May 2021
81
14
6
Jun 2021
27
20
10
Jul 2021
24
21
15
Aug 2021
10
11
9
Sep 2021
31
21
10
Oct 2021
127
28
7
Nov 2021
153
11
9
Dec 2021
201
23
11
Jan 2022
128
19
12
Feb 2022
104
13
8
Mar 2022
169
5
3
Apr 2022
196
9
9
May 2022
196
19
7
Jun 2022
115
10
6
Jul 2022
122
7
4
Aug 2022
173
6
8
Sep 2022
86
12
6
Oct 2022
141
16
7
Nov 2022
144
14
15
Dec 2022
173
7
6
Jan 2023
85
8
6
Feb 2023
79
11
7
Mar 2023
107
12
6
Apr 2023
83
13
10
May 2023
102
12
19
Jun 2023
89
11
5
Jul 2023
153
15
7
Aug 2023
62
6
1
Total
5870
561
353
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