【限定品】 Cause Mutations Loxhd1 Mechanotransduction in Defects 科学・サイエンスの詳細情報
Loxhd1 Mutations Cause Mechanotransduction Defects in。STK11/LKB1-Deficient Phenotype Rather Than Mutation。41467_2019_12947_Fig1_HTML.png。Frontiers | SH-1028, An Irreversible Third-Generation EGFR。