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Q38702643-08593C6E-434B-4A29-A9F8-26F0C6CA8A37
Q38702643-08593C6E-434B-4A29-A9F8-26F0C6CA8A37
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38702643-08593C6E-434B-4A29-A9F8-26F0C6CA8A37
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
P2860
Q38702643-08593C6E-434B-4A29-A9F8-26F0C6CA8A37
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38702643-08593C6E-434B-4A29-A9F8-26F0C6CA8A37
rank
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type
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Statement
wasDerivedFrom
390f2d9e0cfc95599c2f3a3b94862df405206f2e
P2860
Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.