(Q37693369)

English

De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability

scientific article published on 27 March 2014

Statements

De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability (English)
Olivera Spasic-Boskovic
Michael J Parker
Hayley Archer
Soo-Mi Park
Natalie Canham
Susan E Holder
Meredith Wilson
Anna Hackett
Michael Field
James A B Floyd
UK10K Consortium
Matthew Hurles
F Lucy Raymond
27 March 2014
618-624

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