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Volume 58, Issue 5
Novel loss-of-function mutation in HERC2 is associated with severe developmental delay and paediatric lethality
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Genotype-phenotype correlations
Original research
Novel loss-of-function mutation in
HERC2
is associated with severe developmental delay and paediatric lethality
Online download statistics by month:
Online download statistics by month: June 2020 to April 2025
Abstract
Full
Pdf
Jun 2020
391
390
144
Jul 2020
188
184
42
Aug 2020
55
55
23
Sep 2020
92
90
28
Oct 2020
96
97
35
Nov 2020
45
45
15
Dec 2020
69
69
13
Jan 2021
107
107
38
Feb 2021
99
93
34
Mar 2021
111
110
23
Apr 2021
256
255
37
May 2021
190
187
52
Jun 2021
120
117
40
Jul 2021
91
88
28
Aug 2021
109
109
34
Sep 2021
118
117
33
Oct 2021
108
106
33
Nov 2021
110
105
47
Dec 2021
141
144
29
Jan 2022
131
141
33
Feb 2022
114
116
17
Mar 2022
112
112
46
Apr 2022
110
111
30
May 2022
126
129
33
Jun 2022
116
115
34
Jul 2022
93
92
18
Aug 2022
75
74
14
Sep 2022
102
99
26
Oct 2022
136
136
35
Nov 2022
105
108
14
Dec 2022
101
100
13
Jan 2023
93
87
19
Feb 2023
107
109
26
Mar 2023
118
124
22
Apr 2023
117
117
21
May 2023
70
69
19
Jun 2023
66
66
9
Jul 2023
78
80
24
Aug 2023
66
63
18
Sep 2023
115
113
15
Oct 2023
269
270
28
Nov 2023
427
425
58
Dec 2023
109
107
20
Jan 2024
32
33
18
Feb 2024
49
46
23
Mar 2024
63
52
94
Apr 2024
49
51
36
May 2024
54
50
19
Jun 2024
47
47
27
Jul 2024
37
39
19
Aug 2024
41
43
14
Sep 2024
48
44
23
Oct 2024
47
43
23
Nov 2024
79
75
22
Dec 2024
83
83
27
Jan 2025
84
74
29
Feb 2025
65
63
14
Mar 2025
67
64
23
Apr 2025
95
98
29
Total
6392
6336
1760
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