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Q39020440-249957C3-3812-45EC-AFBB-281BC678AAE0
Q39020440-249957C3-3812-45EC-AFBB-281BC678AAE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39020440-249957C3-3812-45EC-AFBB-281BC678AAE0
A novel c132-134del mutation in Unverricht-Lundborg disease and the review of literature of heterozygous compound patients.
P2860
Q39020440-249957C3-3812-45EC-AFBB-281BC678AAE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39020440-249957C3-3812-45EC-AFBB-281BC678AAE0
rank
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type
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Statement
wasDerivedFrom
7833e34d5e390c5f58d08d6ffd25ea74c892e2c5
P2860
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.