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Q58790671-03786CD8-E496-4787-8A99-EFAC31A5AF16
Q58790671-03786CD8-E496-4787-8A99-EFAC31A5AF16
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http://www.wikidata.org/entity/statement/Q58790671-03786CD8-E496-4787-8A99-EFAC31A5AF16
Phenotypic characterization of patients with early-onset high myopia due to mutations in or : Why not Stickler syndrome?
P2860
Q58790671-03786CD8-E496-4787-8A99-EFAC31A5AF16
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58790671-03786CD8-E496-4787-8A99-EFAC31A5AF16
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wasDerivedFrom
508d1ee6ecfd11b82565c2f6b6eea0ca1005dc8d
P2860
A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome.