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Q33617351-2BD55B07-D48C-470B-92AB-B50BFA72B3FD
Q33617351-2BD55B07-D48C-470B-92AB-B50BFA72B3FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33617351-2BD55B07-D48C-470B-92AB-B50BFA72B3FD
X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes
P2860
Q33617351-2BD55B07-D48C-470B-92AB-B50BFA72B3FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33617351-2BD55B07-D48C-470B-92AB-B50BFA72B3FD
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Statement
wasDerivedFrom
7aabb25ff7d764e6a9b4c127f00e5c5120850115
P2860
Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans.