Journal Articles
Human Mutation
Year : 2018
Olena Pylypenko : Connect in order to contact the contributor
https://hal.science/hal-02349537
Submitted on : Tuesday, November 5, 2019-4:59:30 PM
Last modification on : Friday, March 24, 2023-2:53:13 PM
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- HAL Id : hal-02349537 , version 1
- DOI : 10.1002/humu.23386
- PUBMEDCENTRAL : PMC5838515
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Herschel Dhekne, Olena Pylypenko, Arend Overeem, Rosaria Ferreira, K. Joeri van Der Velde, et al.. MYO5B , STX3 , and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Human Mutation, 2018, 39 (3), pp.333-344. ⟨10.1002/humu.23386⟩. ⟨hal-02349537⟩
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