Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

Rare variants in PRKCI linked to Van der Woude syndrome (1 in 35k births) reveal new insights into peridermopathy. #Genetics科研 PMID:40902599, Am J Hum Genet 2025, @AJHGNews https://t.co/eHLTzZfgKa #AI #Pharma #BioMed #RNA #ASHG #ESHG

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy #RareDisease #Genetics #morbidgene https://t.co/ep4BZafKUk

📣New from Robinson et al! 📄Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy https://t.co/VgYEhYlqIB