Loss of the arginine methyltranserase PRMT7 causes syndromic intellectual disability with microcephaly and brachydactyly.
Journal article published in 2016 by
Kernohan Kd,
K. D. Kernohan,
A. McBride,
Y. Xi,
N. Martin,
J. Schwartzentruber 
,
Dyment Da,
D. A. Dyment,
J. Majewski,
S. Blaser,
Care4Rare Canada Consortium,
K. M. Boycott,
Boycott Km,
D. Chitayat
,
Dyment Da,
D. A. Dyment,
J. Majewski,
S. Blaser,
Care4Rare Canada Consortium,
K. M. Boycott,
Boycott Km,
D. Chitayat
This paper is made freely available by the publisher.
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