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

Erstveröffentlichung
2018Authors
Dhekne, Herschel S.
Pylypenko, Olena
Overeem, Arend W.
Ferreira, Rosaria J.
van der Velde, K. Joeri
Wissenschaftlicher Artikel
Published in
Human Mutation ; 39 (2018), 3. - S. 333-344. - ISSN 1059-7794. - eISSN 1098-1004