Nagai-Tanima et al., 2020 - Rare hypomorphic human variation in the heptahelical domain of SMO contributes to holoprosencephaly phenotypes. Human Mutation   41(12):2105-2118 Full text @ Hum. Mutat.
Morpholino List (2 Records)
Target Reagent
ptch1 MO1-ptch1
ptch2 MO1-ptch2
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.