WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome.

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

Author/s

author: Vivian Pan, Katherine L Helbig, Hilary J Vernon, Marwan Shinawi, Jane Juusola

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Publication date

August 11, 2015

Language

English

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