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Q40985645-12B4ED57-10A5-4267-A51E-D1369744E7EB
Q40985645-12B4ED57-10A5-4267-A51E-D1369744E7EB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40985645-12B4ED57-10A5-4267-A51E-D1369744E7EB
Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B).
P2860
Q40985645-12B4ED57-10A5-4267-A51E-D1369744E7EB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40985645-12B4ED57-10A5-4267-A51E-D1369744E7EB
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type
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Statement
wasDerivedFrom
79a86a7b9ef2a63565286285e3f1f766e429b322
P2860
Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism