MYO5B, STX3 and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update (Q47269140)
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scientific article published on 21 December 2017
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | MYO5B, STX3 and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update |
scientific article published on 21 December 2017 |
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1 reference
MYO5B, STX3 and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update (English)
1 reference
Arend W Overeem
Malik Zibouche
Rosaria J Ferreira
K Joeri van der Velde
Edmond H H M Rings
Peter van der Sluijs
Morris A Swertz
17 January 2018
1 reference
1 March 2018
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20 June 2019
30 June 2019
14 September 2019
28 September 2019
16 November 2019
11 December 2019
15 December 2019
23 July 2020
6 November 2020
10 references
20 June 2019
30 June 2019
14 September 2019
28 September 2019
16 November 2019
11 December 2019
15 December 2019
23 July 2020
10 September 2020
6 November 2020