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KCNJ11 gene knockout of the Kir6.2 K ATP channel causes maladaptive remodeling and heart failure in hypertension

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CYP11B1 Mutations Causing Non-Classic Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency

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Sequence-specific stalling of DNA polymerase  and the effects of mutations causing progressive ophthalmoplegia

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Transgenic Drosophila models of Noonan syndrome causing PTPN11 gain-of-function mutations

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