MYO5B,STX3, andSTXBP2mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update

Auteurs

Herschel S. Dhekne, Olena Pylypenko, Arend W. Overeem, Rosaria J. Ferreira, K. Joeri van der Velde, Edmond H.H.M. Rings, Carsten Posovszky, Morris A. Swertz, Anne Houdusse, Sven C.D. van IJzendoorn