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

First Author: Singh T

Attributed to: MRC Centre for Neuropsychiatric Genetics and Genomics 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