Leiden University Scholarly Publications

Dhekne, H.S.; Pylypenko, O.; Overeem, A.W.; Ferreira, R.J.; Velde, K.J. van der; Rings, E.H.H.M.; ... ; IJzendoorn, S.C.D. van 2018

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

Article / Letter to editor

open access