De novo MYH9 mutation in congenital scalp hemangioma
Fomchenko EI, Duran D, Jin SC, Dong W, Erson-Omay EZ, Antwi P, Allocco A, Gaillard JR, Huttner A, Gunel M, DiLuna ML, Kahle KT. De novo MYH9 mutation in congenital scalp hemangioma. Molecular Case Studies 2018, 4: a002998. PMID: 29903892, PMCID: PMC6071566, DOI: 10.1101/mcs.a002998.Peer-Reviewed Original ResearchMeSH KeywordsFemaleGerm-Line MutationHemangiomaHumansInfant, NewbornLoss of Function MutationMolecular Motor ProteinsMyosin Heavy ChainsScalpSkin NeoplasmsConceptsRegulator of cytokinesis