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Q42661057-3F341B54-E10A-409F-8B9B-C0B648FCF5C6
Q42661057-3F341B54-E10A-409F-8B9B-C0B648FCF5C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42661057-3F341B54-E10A-409F-8B9B-C0B648FCF5C6
In silico study of Alzheimer's disease in relation to FYN gene.
P2860
Q42661057-3F341B54-E10A-409F-8B9B-C0B648FCF5C6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42661057-3F341B54-E10A-409F-8B9B-C0B648FCF5C6
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Statement
wasDerivedFrom
0fd99f341a4bcccdf88cdda94aee4e4038d3a8b7
P2860
Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation.