MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update

Erstveröffentlichung

2018

Authors

Dhekne, Herschel S.

Pylypenko, Olena

Overeem, Arend W.

Ferreira, Rosaria J.

van der Velde, K. Joeri

et al.

Wissenschaftlicher Artikel

Published in

Human Mutation ; 39 (2018), 3. - S. 333-344. - ISSN 1059-7794. - eISSN 1098-1004

Link to publication

https://dx.doi.org/10.1002/humu.23386

Institutions

UKU. Klinik für Kinder- und Jugendmedizin

Subject headings

[DDC subject group]: DDC 570 / Life sciences | DDC 610 / Medicine & health

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Metadata

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