MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update (vol 39, pg 333, 2017)

Dhekne, H. S., Pylypenko, O., Overeem, A. W., Zibouche, M., Ferreira, R. J., van der Velde, K. J., Rings, E. H. H. M., Posovszky, C., van der Sluijs, P., Swertz, M. A., Houdusse, A. & van IJzendoorn, S. C. D., Oct-2018, In : Human Mutation. 39, 10, p. 1468 1 p.

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Original languageEnglish
Pages (from-to)1468
Number of pages1
JournalHuman Mutation
Issue number10
Publication statusPublished - Oct-2018

ID: 66165369