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Q32073748-3B929AF9-C2F5-4F09-8595-1100A5FD71E8
Q32073748-3B929AF9-C2F5-4F09-8595-1100A5FD71E8
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http://www.wikidata.org/entity/statement/Q32073748-3B929AF9-C2F5-4F09-8595-1100A5FD71E8
Structure of the human biotinidase gene.
P2860
Q32073748-3B929AF9-C2F5-4F09-8595-1100A5FD71E8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q32073748-3B929AF9-C2F5-4F09-8595-1100A5FD71E8
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0eb8feb56f250436a83cf2db5e8b9b13053a1fc8
P2860
Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States.