Search

Author/Creator Dhekne, Herschel S.

1. An Overview and Online Registry of Microvillus Inclusion Disease Patients and their MYO5B Mutations. Issue 12 (16th October 2013)

Authors:
van der, K. Joeri; Dhekne, Herschel S.; Swertz, Morris A.; Sirigu, Serena; Ropars, Virginie; Vinke, Petra C.; Rengaw, Trebor; van den, Peter C.; Rings, Edmond H. H. M.; Houdusse, Anne; van, Sven C. D.
Journal:
Human mutation
Issue:
Volume 34:Issue 12(2013:Dec.)
Page Start:
1597
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Issue 3 (17th January 2018)

Authors:
Dhekne, Herschel S.; Pylypenko, Olena; Overeem, Arend W.; Ferreira, Rosaria J.; van der Velde, K. Joeri; Rings, Edmond H.H.M.; Posovszky, Carsten; Swertz, Morris A.; Houdusse, Anne; van IJzendoorn, Sven C.D.
Journal:
Human mutation
Issue:
Volume 39:Issue 3(2018)
Page Start:
333
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

Limit your search