De novoand rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder-Reference-Cited by-同舟云学术

De novoand rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder

Published:2014-09-16 Issue:11 Volume:51 Page:737-747
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Babbs Christian,Lloyd Deborah,Pagnamenta Alistair T,Twigg Stephen R F,Green Joanne,McGowan Simon J,Mirza Ghazala,Naples Rebecca,Sharma Vikram P,Volpi Emanuela V,Buckle Veronica J,Wall Steven A,Knight Samantha J L,Parr Jeremy R,Wilkie Andrew O M,

Publisher

BMJ

Subject

Genetics(clinical),Genetics

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