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1
Q33800041-76E1368D-E23E-472F-BAB9-FC36114B1CC0
Q33800041-76E1368D-E23E-472F-BAB9-FC36114B1CC0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33800041-76E1368D-E23E-472F-BAB9-FC36114B1CC0
SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis
P2860
Q33800041-76E1368D-E23E-472F-BAB9-FC36114B1CC0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33800041-76E1368D-E23E-472F-BAB9-FC36114B1CC0
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Statement
wasDerivedFrom
56d56e17342bb4356a699fd000c077ad7ca5bc84
P2860
Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype.