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
Metadata
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