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Volume 91, Issue 3
Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2
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Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2
Online download statistics by month:
Online download statistics by month: August 2019 to February 2024
Abstract
Full
Pdf
Aug 2019
720
66
25
Sep 2019
479
37
20
Oct 2019
253
29
9
Nov 2019
171
10
2
Dec 2019
268
36
13
Jan 2020
269
45
20
Feb 2020
954
43
17
Mar 2020
370
30
16
Apr 2020
143
15
10
May 2020
126
20
9
Jun 2020
116
20
12
Jul 2020
124
16
9
Aug 2020
128
22
8
Sep 2020
175
16
8
Oct 2020
116
7
4
Nov 2020
119
12
10
Dec 2020
91
6
4
Jan 2021
107
11
9
Feb 2021
107
10
9
Mar 2021
269
21
22
Apr 2021
105
11
8
May 2021
42
3
2
Jun 2021
12
9
7
Jul 2021
11
3
2
Aug 2021
12
8
4
Sep 2021
17
8
1
Oct 2021
156
16
9
Nov 2021
84
9
8
Dec 2021
102
15
6
Jan 2022
94
9
6
Feb 2022
91
3
3
Mar 2022
74
13
6
Apr 2022
89
18
10
May 2022
88
8
3
Jun 2022
104
10
4
Jul 2022
54
7
1
Aug 2022
85
11
2
Sep 2022
104
3
3
Oct 2022
121
16
10
Nov 2022
74
8
4
Dec 2022
105
5
1
Jan 2023
128
17
12
Feb 2023
170
9
1
Mar 2023
79
6
1
Apr 2023
59
12
4
May 2023
73
2
2
Jun 2023
84
7
7
Jul 2023
54
7
3
Aug 2023
63
12
8
Sep 2023
53
5
2
Oct 2023
76
11
5
Nov 2023
85
7
3
Dec 2023
63
4
4
Jan 2024
79
7
6
Feb 2024
56
6
5
Total
7851
777
399
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