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De novo mutations of SCN1A are responsible for arthrogryposis broadening the SCN1A-related phenotypes
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Neurogenetics
Original research
De novo mutations of
SCN1A
are responsible for arthrogryposis broadening the
SCN1A
-related phenotypes
Online download statistics by month:
Online download statistics by month: September 2020 to February 2021
Abstract
Full
Pdf
Sep 2020
663
42
32
Oct 2020
332
29
11
Nov 2020
219
48
12
Dec 2020
260
256
30
Jan 2021
114
107
15
Feb 2021
167
167
19
Total
1755
649
119
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