Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders (2016)

First Author: Singh T
Attributed to:  Molecular Genetic Studies of Schizophrenia funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/036384

Publication URI: http://dx.doi.org/10.1101/036384

Type: Preprint