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(1 - 2 of 2)
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
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
The role of enterocyte defects in the pathogenesis of congenital diarrheal disorders
Overeem, A.W.; Posovszky, C.; Rings, E.H.M.M.; Giepmans, B.N.G.; IJzendoorn, S.C.D. van 2016
The role of enterocyte defects in the pathogenesis of congenital diarrheal disorders
Article / Letter to editor
metadata only