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Q24612792-1880A69B-5984-444C-8BB9-CCE0DF34108D
Q24612792-1880A69B-5984-444C-8BB9-CCE0DF34108D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24612792-1880A69B-5984-444C-8BB9-CCE0DF34108D
The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)
P2860
Q24612792-1880A69B-5984-444C-8BB9-CCE0DF34108D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24612792-1880A69B-5984-444C-8BB9-CCE0DF34108D
rank
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wasDerivedFrom
8f6b91671905ce5a1cd4c6a6bd2186520ab7c28b
P2860
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms