Further delineation of the phenotype caused by loss of function mutations in PRMT7.
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DOI: 10.1016/j.ejmg.2018.07.007
Abstract: PRMT7 encodes for an arginine methyltransferase that methylates arginine residues on various protein substrates and has been shown to play a role in various developmental processes. Mutations in PRMT7 have been recently shown to be… read more here.
Keywords: mutations prmt7; phenotype; phenotype caused; delineation phenotype ... See more keywords