Start Date
2022
Description
- BCS1L is a mitochondrial protein that assists in building complex III of the electron transport chain which allows for cellular respiration to occur
- Different mutations in BCS1L can result in three rare genetic diseases: Bjornstad Syndrome, BCS1L Mitopathy, or GRACILE Syndrome
Recommended Citation
Pastoor, Emma; Wilstermann, Amy; and Baker, Rachael, "Investigating Replacement of a Yeast Gene with a Human Gene as a Rare Disease Model System" (2022). Summer Research. 32.
https://digitalcommons.calvin.edu/summer_research/2022/Posters/32
Included in
Jan 1st, 12:00 AM
Investigating Replacement of a Yeast Gene with a Human Gene as a Rare Disease Model System
- BCS1L is a mitochondrial protein that assists in building complex III of the electron transport chain which allows for cellular respiration to occur
- Different mutations in BCS1L can result in three rare genetic diseases: Bjornstad Syndrome, BCS1L Mitopathy, or GRACILE Syndrome