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MINK1 activates SCN5A. 1 / 1

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"These studies indicate that, as in KVLQT1, mutations in minK can cause both autosomal dominant (Romano-Ward syndrome) and autosomal-recessive (JLN) LQT.Identification of SCN5A, HERG, KVLQT1 and minK a[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

9791861

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IndraLab

Statements

MINK1 activates SCN5A. 1 / 1

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