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Volume 58, Issue 11
De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes
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Neurogenetics
Original research
De novo mutations of
SCN1A
are responsible for arthrogryposis broadening the
SCN1A
-related phenotypes
Online download statistics by month:
Online download statistics by month: September 2020 to March 2024
Abstract
Full
Pdf
Sep 2020
663
42
32
Oct 2020
332
29
11
Nov 2020
219
48
12
Dec 2020
260
256
30
Jan 2021
114
107
15
Feb 2021
167
167
19
Mar 2021
85
82
18
Apr 2021
98
93
9
May 2021
111
111
24
Jun 2021
88
89
25
Jul 2021
110
105
35
Aug 2021
90
85
18
Sep 2021
105
97
42
Oct 2021
252
245
55
Nov 2021
248
246
85
Dec 2021
100
94
38
Jan 2022
94
94
37
Feb 2022
122
111
38
Mar 2022
107
107
30
Apr 2022
70
71
19
May 2022
84
85
24
Jun 2022
54
52
13
Jul 2022
53
56
21
Aug 2022
66
64
20
Sep 2022
88
86
21
Oct 2022
61
59
8
Nov 2022
58
54
24
Dec 2022
25
26
11
Jan 2023
33
30
20
Feb 2023
48
46
30
Mar 2023
34
27
9
Apr 2023
44
42
9
May 2023
24
21
16
Jun 2023
28
24
12
Jul 2023
40
35
15
Aug 2023
54
42
13
Sep 2023
34
34
11
Oct 2023
38
34
16
Nov 2023
55
52
11
Dec 2023
41
39
10
Jan 2024
53
47
14
Feb 2024
29
24
11
Mar 2024
36
32
28
Total
4515
3290
959
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