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Q24564863-888D1BE3-8798-42AA-9CC9-16A48A928EAD
Q24564863-888D1BE3-8798-42AA-9CC9-16A48A928EAD
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http://www.wikidata.org/entity/statement/Q24564863-888D1BE3-8798-42AA-9CC9-16A48A928EAD
Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia
P2860
Q24564863-888D1BE3-8798-42AA-9CC9-16A48A928EAD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24564863-888D1BE3-8798-42AA-9CC9-16A48A928EAD
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wasDerivedFrom
2be358d1fceca43f05578b71fb59cc881de3e8ad
P2860
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.