PRMT7

Publications

Akawi N et al. Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families. Nat Genet. 2015;47(11):1363-9. PMID: 26437029.

Birnbaum R et al. Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations. Am J Med Genet A. 2019;179(1):78-84. PMID: 30513135.

Jain K et al. PRMT7 as a unique member of the protein arginine methyltransferase family: A review. Arch Biochem Biophys. 2019;665:36-45. PMID: 30802433.

Kernohan KD et al. Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly. Clin Genet. 2017;91(5):708-16. PMID: 27718516.