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Q52150811-8DF1A983-4FFF-488B-990E-68B26F67F189
Q52150811-8DF1A983-4FFF-488B-990E-68B26F67F189
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52150811-8DF1A983-4FFF-488B-990E-68B26F67F189
Reply: ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.
P2860
Q52150811-8DF1A983-4FFF-488B-990E-68B26F67F189
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52150811-8DF1A983-4FFF-488B-990E-68B26F67F189
rank
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type
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wasDerivedFrom
79c429e5f2e9dccccbfdf3ed32af18bbf76f85a6
P2860
Understanding pyrroline-5-carboxylate synthetase deficiency: clinical, molecular, functional, and expression studies, structure-based analysis, and novel therapy with arginine