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- NP899109.RA2xeKEBt8UOg0C_mXQKfq4-_M47xZeWqHm5YwW5kmxDs130_assertion type Assertion NP899109.RA2xeKEBt8UOg0C_mXQKfq4-_M47xZeWqHm5YwW5kmxDs130_head.
- NP899109.RA2xeKEBt8UOg0C_mXQKfq4-_M47xZeWqHm5YwW5kmxDs130_assertion description "[Important advances made in the past year have included identification of KCNJ5 potassium channel mutations in the pathogenesis of both aldosterone-producing adenomas and familial hyperaldosteronism type III; characterization of phosphodiesterase 11A as a modifier of phenotype in Carney complex caused by protein kinase, cAMP-dependent, regulatory subunit, type-I mutations; the finding of 11?-hydroxysteroid dehydrogenase type I mutations as a novel mechanism for cortisone reductase deficiency; and demonstration of potential mortality benefit in pursuing comprehensive presymptomatic screening for patients with Li-Fraumeni syndrome, including possible reduction in risks associated with adrenocortical carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899109.RA2xeKEBt8UOg0C_mXQKfq4-_M47xZeWqHm5YwW5kmxDs130_provenance.
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- NP899109.RA2xeKEBt8UOg0C_mXQKfq4-_M47xZeWqHm5YwW5kmxDs130_assertion wasGeneratedBy ECO_0000203 NP899109.RA2xeKEBt8UOg0C_mXQKfq4-_M47xZeWqHm5YwW5kmxDs130_provenance.