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BMJ Journals
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Volume 53, Issue 11
Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS
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Developmental defects
Original article
Mutations in
MYT1
, encoding the myelin transcription factor 1, are a rare cause of OAVS
Online download statistics by month:
Online download statistics by month: June 2016 to April 2023
Abstract
Full
Pdf
Jun 2016
166
5
9
Jul 2016
254
41
53
Aug 2016
97
17
16
Sep 2016
174
35
27
Oct 2016
421
45
30
Nov 2016
629
29
64
Dec 2016
126
44
33
Jan 2017
126
9
13
Feb 2017
101
27
14
Mar 2017
142
21
11
Apr 2017
108
27
13
May 2017
41
24
9
Jun 2017
61
11
5
Jul 2017
87
15
5
Aug 2017
125
18
7
Sep 2017
94
16
7
Oct 2017
131
10
4
Nov 2017
108
10
5
Dec 2017
131
16
16
Jan 2018
241
25
25
Feb 2018
182
17
6
Mar 2018
262
15
5
Apr 2018
150
14
5
May 2018
128
5
2
Jun 2018
131
9
4
Jul 2018
65
10
4
Aug 2018
76
8
6
Sep 2018
70
10
3
Oct 2018
119
11
4
Nov 2018
135
8
8
Dec 2018
96
6
0
Jan 2019
93
7
2
Feb 2019
113
13
8
Mar 2019
77
15
4
Apr 2019
63
10
5
May 2019
68
13
6
Jun 2019
88
10
3
Jul 2019
51
11
3
Aug 2019
87
4
0
Sep 2019
53
6
4
Oct 2019
83
10
4
Nov 2019
59
3
2
Dec 2019
53
9
7
Jan 2020
96
9
4
Feb 2020
90
9
3
Mar 2020
60
5
2
Apr 2020
55
9
4
May 2020
53
3
1
Jun 2020
98
2
6
Jul 2020
48
6
2
Aug 2020
47
10
6
Sep 2020
88
11
4
Oct 2020
71
3
2
Nov 2020
59
2
2
Dec 2020
59
3
3
Jan 2021
45
3
0
Feb 2021
58
6
4
Mar 2021
78
2
2
Apr 2021
78
2
1
May 2021
37
4
3
Jun 2021
6
5
1
Jul 2021
4
4
4
Aug 2021
7
6
6
Sep 2021
13
12
2
Oct 2021
84
10
6
Nov 2021
101
0
3
Dec 2021
61
10
5
Jan 2022
86
4
1
Feb 2022
81
6
3
Mar 2022
53
3
2
Apr 2022
135
5
4
May 2022
151
8
5
Jun 2022
97
7
3
Jul 2022
103
11
9
Aug 2022
122
8
1
Sep 2022
106
2
0
Oct 2022
98
14
9
Nov 2022
87
6
5
Dec 2022
38
7
3
Jan 2023
114
9
4
Feb 2023
109
9
3
Mar 2023
60
5
2
Apr 2023
94
10
3
Total
8595
919
594
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