WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome.
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| Description | scientific article published on 11 August 2015 |
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author: Vivian Pan Jane Juusola Hilary J Vernon Katherine L Helbig Marwan Shinawi |
| Publication date | August 11, 2015 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |