AMBRA1 P.gln30arg Mutation, Identified in a Cowden Syndrome Family, Exhibits Hyperproliferative Potential in Htert-Rpe1 Cells
International Journal of Molecular Sciences（2022）
Key words
AMBRA1,AMBRA1 Q30R mutant,Cowden syndrome,primary cilia,CRISPR,Cas,G1,S transition
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