https://sb242235inhibitor.com/....thickness-involving-
OUTCOMES Genetic analysis identified a novel SCNN1G missense variant (c.1874CT, p.Pro625Leu) within the proband with LS in youth. In silico analysis revealed this heterozygous variation was very conserved and deleterious. A total of 38 journals described pediatric LS associated with 25 pathogenic alternatives in SCNN1B and SCNN1G in 54 children. Regardless of the phenotypic heterogeneity, early-onset high blood pressure is considered the most common feature. All LS
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