Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly
K.D. Kernohan; A. McBride; Y. Xi; N. Martin; J. Schwartzentruber; D.A. Dyment; J. Majewski; S. Blaser; K.M. Boycott; D. Chitayat
Author Information: Children's Hospital of Eastern Ontario Research Institute
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