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Q48231638-E66666B7-8B03-4F18-9A71-BBB3ABE3D57D
Q48231638-E66666B7-8B03-4F18-9A71-BBB3ABE3D57D
BestRank
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http://www.wikidata.org/entity/statement/Q48231638-E66666B7-8B03-4F18-9A71-BBB3ABE3D57D
Novel recessive mutations in MSTO1 cause cerebellar atrophy with pigmentary retinopathy.
P2860
Q48231638-E66666B7-8B03-4F18-9A71-BBB3ABE3D57D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48231638-E66666B7-8B03-4F18-9A71-BBB3ABE3D57D
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wasDerivedFrom
a724fcc08e261d80b6ba7b0bb1cca3a99499c464
P2860
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome.