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Q35140432-BF66946A-6859-454D-8775-BB6F6918C6A9
Q35140432-BF66946A-6859-454D-8775-BB6F6918C6A9
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http://www.wikidata.org/entity/statement/Q35140432-BF66946A-6859-454D-8775-BB6F6918C6A9
Mutation spectrum of six genes in Chinese phenylketonuria patients obtained through next-generation sequencing.
P2860
Q35140432-BF66946A-6859-454D-8775-BB6F6918C6A9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35140432-BF66946A-6859-454D-8775-BB6F6918C6A9
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wasDerivedFrom
4f8cafdc55a34e7df33a7abb9bd0e95978560000
P2860
GTP cyclohydrolase I deficiency, a new enzyme defect causing hyperphenylalaninemia with neopterin, biopterin, dopamine, and serotonin deficiencies and muscular hypotonia.