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1
4052b26d55981f34d983c1608b050ea84e86bdd9
4052b26d55981f34d983c1608b050ea84e86bdd9
Reference
http://www.wikidata.org/reference/4052b26d55981f34d983c1608b050ea84e86bdd9
Q55784970-CE107283-41BE-408A-B9FB-7A71E42EEBF2
wasDerivedFrom
4052b26d55981f34d983c1608b050ea84e86bdd9
Reference
http://www.wikidata.org/reference/4052b26d55981f34d983c1608b050ea84e86bdd9
type
Reference
P248
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome.