TY  - GEN
AU  - Grozeva,Detelina
AU  - Carss,Keren
AU  - Spasic-Boskovic,Olivera
AU  - Parker,Michael J
AU  - Archer,Hayley
AU  - Firth,Helen V
AU  - Park,Soo-Mi
AU  - Canham,Natalie
AU  - Holder,Susan E
AU  - Wilson,Meredith
AU  - Hackett,Anna
AU  - Field,Michael
AU  - Floyd,James A B
AU  - Hurles,Matthew
AU  - Raymond,F Lucy
TI  - De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability
SN  - 1537-6605
PY  - 2014///0530
KW  - Adolescent
KW  - Child
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 3
KW  - Humans
KW  - Intellectual Disability
KW  - genetics
KW  - Male
KW  - Methyltransferases
KW  - Mutation
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2014.03.006
ER  -