Cite
HARVARD Citation
Dhekne, H. et al. (2018). MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Human mutation. 39 (3), pp. 333-344. [Online].
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Dhekne, H. et al. (2018). MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update. Human mutation. 39 (3), pp. 333-344. [Online].