Persistent URL of this record https://hdl.handle.net/1887/74933
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MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
- All authors
- Dhekne, H.S.; Pylypenko, O.; Overeem, A.W.; Ferreira, R.J.; Velde, K.J. van der; Rings, E.H.H.M.; Posovszky, C.; Swertz, M.A.; Houdusse, A.; IJzendoorn, S.C.D. van
- Date
- 2018-03-31
- Journal
- Human Mutation
- Volume
- 39
- Issue
- 3
- Pages
- 333 - 344