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Volume 55, Issue 5
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss
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Novel disease loci
Original Article
Mutation of
IFNLR1
, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss
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Online download statistics by month: March 2018 to February 2024
Abstract
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Pdf
Feb 2018
453
452
120
Mar 2018
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313
64
Apr 2018
375
377
94
May 2018
291
293
51
Jun 2018
115
123
22
Jul 2018
126
126
21
Aug 2018
83
83
20
Sep 2018
77
77
14
Oct 2018
49
49
13
Nov 2018
92
92
24
Dec 2018
82
82
15
Jan 2019
47
47
16
Feb 2019
42
29
16
Mar 2019
40
37
20
Apr 2019
40
34
15
May 2019
45
43
12
Jun 2019
33
29
16
Jul 2019
56
47
25
Aug 2019
93
88
22
Sep 2019
97
96
17
Oct 2019
45
43
20
Nov 2019
43
43
8
Dec 2019
38
38
5
Jan 2020
54
50
7
Feb 2020
26
24
14
Mar 2020
49
47
30
Apr 2020
24
23
37
May 2020
35
31
19
Jun 2020
39
33
17
Jul 2020
30
27
11
Aug 2020
36
31
13
Sep 2020
36
25
19
Oct 2020
37
33
25
Nov 2020
48
41
17
Dec 2020
38
38
9
Jan 2021
34
29
15
Feb 2021
28
22
17
Mar 2021
34
27
22
Apr 2021
33
30
22
May 2021
34
33
11
Jun 2021
27
24
12
Jul 2021
36
35
15
Aug 2021
29
27
16
Sep 2021
38
35
25
Oct 2021
30
26
30
Nov 2021
33
25
39
Dec 2021
53
50
30
Jan 2022
20
18
12
Feb 2022
26
21
14
Mar 2022
32
28
14
Apr 2022
44
43
15
May 2022
58
53
35
Jun 2022
44
43
23
Jul 2022
30
32
6
Aug 2022
51
40
10
Sep 2022
34
32
13
Oct 2022
46
40
17
Nov 2022
32
29
18
Dec 2022
43
34
16
Jan 2023
27
25
14
Feb 2023
28
27
14
Mar 2023
32
32
16
Apr 2023
22
23
22
May 2023
26
23
14
Jun 2023
24
20
14
Jul 2023
41
38
25
Aug 2023
19
20
9
Sep 2023
35
34
8
Oct 2023
48
45
14
Nov 2023
26
22
8
Dec 2023
56
55
24
Jan 2024
52
25
12
Feb 2024
39
37
16
Total
4453
4246
1525
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