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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 December 2020
Abstract
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Pdf
Sep 2020
663
42
32
Oct 2020
332
29
11
Nov 2020
219
48
12
Dec 2020
260
256
30
Total
1474
375
85
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