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Volume 56, Issue 11
Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms
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Original research
Truncating mutations in exons 20 and 21 of
OFD1
can cause primary ciliary dyskinesia without associated syndromic symptoms
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Abstract
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Jul 2019
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Aug 2019
654
68
26
Sep 2019
304
20
6
Oct 2019
510
37
19
Nov 2019
292
43
22
Dec 2019
165
17
13
Jan 2020
160
21
10
Feb 2020
126
8
4
Mar 2020
91
14
2
Apr 2020
80
12
9
May 2020
123
16
9
Jun 2020
101
10
5
Jul 2020
139
4
4
Aug 2020
100
8
5
Sep 2020
94
6
1
Oct 2020
93
3
0
Nov 2020
96
8
4
Dec 2020
148
8
9
Jan 2021
119
7
9
Feb 2021
120
15
7
Mar 2021
100
6
5
Apr 2021
65
7
3
May 2021
32
5
3
Jun 2021
26
20
5
Jul 2021
19
16
8
Aug 2021
11
12
4
Sep 2021
9
7
2
Oct 2021
133
8
4
Nov 2021
95
14
3
Dec 2021
72
3
4
Jan 2022
92
7
7
Feb 2022
100
19
5
Mar 2022
144
9
5
Apr 2022
119
4
0
May 2022
99
5
0
Jun 2022
109
9
2
Jul 2022
54
3
3
Aug 2022
83
12
2
Sep 2022
169
12
7
Oct 2022
94
11
4
Nov 2022
106
8
6
Dec 2022
48
5
4
Jan 2023
176
6
3
Feb 2023
118
7
1
Mar 2023
155
8
4
Apr 2023
78
3
2
May 2023
62
12
2
Jun 2023
69
11
7
Jul 2023
81
10
3
Aug 2023
106
12
5
Sep 2023
81
2
4
Oct 2023
105
12
2
Nov 2023
121
15
4
Dec 2023
91
7
4
Jan 2024
91
8
7
Feb 2024
114
9
5
Mar 2024
58
7
0
Total
6899
659
303
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