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Volume 60, Issue 9
Pathogenic variations in MAML2 and MAMLD1 contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway
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Genotype-phenotype correlations
Original research
Pathogenic variations in
MAML2
and
MAMLD1
contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathway
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Online download statistics by month: March 2023 to November 2023
Abstract
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Pdf
Mar 2023
531
36
22
Apr 2023
186
17
10
May 2023
202
9
1
Jun 2023
134
7
3
Jul 2023
144
14
2
Aug 2023
300
24
8
Sep 2023
254
20
11
Oct 2023
137
11
7
Nov 2023
112
6
4
Total
2000
144
68
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