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Q50335717-05E2AB8D-74F7-49B7-991A-4EACE37642E1
Q50335717-05E2AB8D-74F7-49B7-991A-4EACE37642E1
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http://www.wikidata.org/entity/statement/Q50335717-05E2AB8D-74F7-49B7-991A-4EACE37642E1
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.
P2860
Q50335717-05E2AB8D-74F7-49B7-991A-4EACE37642E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50335717-05E2AB8D-74F7-49B7-991A-4EACE37642E1
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wasDerivedFrom
77d805dc2a2c94143560b2d329222c233cd29657
P2860
Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.