WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome. (Q38564668)
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scientific article published on 11 August 2015
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome. |
scientific article published on 11 August 2015 |
Statements
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome (English)
Cori DeSanto
Kristin D'Aco
Gabriel C Araujo
Nora Shannon
DDD Study
April Rahrig
Kristin G Monaghan
Zhiyv Niu
Patrik Vitazka
Jonathan Dodd
Sha Tang
Linda Manwaring
Arelis Martir-Negron
Rhonda E Schnur
Audrey Schroeder
Bethany Friedman
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