Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study (2016)

First Author: McRae J

Attributed to: Investigating the biology of mitochondrial DNA disease transmission to enable affected families to have healthy children funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/049056

Publication URI: http://dx.doi.org/10.1101/049056

Type: Preprint