Cite
HARVARD Citation
Kernohan, K. et al. (2017). Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly. Clinical genetics. 91 (5), pp. 708-716. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Kernohan, K. et al. (2017). Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly. Clinical genetics. 91 (5), pp. 708-716. [Online].