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Q24310789-15B24F21-1A19-4256-98A9-6E099ED1AA31
Q24310789-15B24F21-1A19-4256-98A9-6E099ED1AA31
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24310789-15B24F21-1A19-4256-98A9-6E099ED1AA31
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome
P1476
Q24310789-15B24F21-1A19-4256-98A9-6E099ED1AA31
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24310789-15B24F21-1A19-4256-98A9-6E099ED1AA31
rank
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type
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Statement
wasDerivedFrom
02c121ac8ac37e994cd7498bf8238c706757242f
P1476
A homozygous mutation in human
......
lonus epilepsy-ataxia syndrome
@en