IndraLab

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Mutated USP6 inhibits mis4. 1 / 1

| 1

reach

"In addition, Mis4 human homolog NIPBL is the causal gene of Cornelia de Lange syndrome (57, 58), and the suppression of mis4 by hrp1 mutations may offer clues to treat the disease."

31072933

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IndraLab

Statements

Mutated USP6 inhibits mis4. 1 / 1

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