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Q24337555-98202585-3595-43ED-B00C-384040B4DA79
Q24337555-98202585-3595-43ED-B00C-384040B4DA79
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http://www.wikidata.org/entity/statement/Q24337555-98202585-3595-43ED-B00C-384040B4DA79
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia
P2860
Q24337555-98202585-3595-43ED-B00C-384040B4DA79
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24337555-98202585-3595-43ED-B00C-384040B4DA79
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wasDerivedFrom
937137331026c042d4c730b68f87d81068315278
P2860
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant