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Q33576824-34E0CA65-099B-460D-A58B-2E66B8C0D1CF
Q33576824-34E0CA65-099B-460D-A58B-2E66B8C0D1CF
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http://www.wikidata.org/entity/statement/Q33576824-34E0CA65-099B-460D-A58B-2E66B8C0D1CF
Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy.
P2860
Q33576824-34E0CA65-099B-460D-A58B-2E66B8C0D1CF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33576824-34E0CA65-099B-460D-A58B-2E66B8C0D1CF
rank
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type
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wasDerivedFrom
a0bfe14985bcd97b77f412872a573582e42ac81a
P2860
Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.