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Q46352293-47360B2E-3403-4EF9-B1F8-7D6EC1B521D8
Q46352293-47360B2E-3403-4EF9-B1F8-7D6EC1B521D8
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http://www.wikidata.org/entity/statement/Q46352293-47360B2E-3403-4EF9-B1F8-7D6EC1B521D8
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
P2860
Q46352293-47360B2E-3403-4EF9-B1F8-7D6EC1B521D8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46352293-47360B2E-3403-4EF9-B1F8-7D6EC1B521D8
rank
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type
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wasDerivedFrom
5cb3883fc8d56feaa8feeeca1b98dfddb92fa72d
P2860
GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.