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Q34775800-674E3BED-5719-4193-B8A8-B8C036014370
Q34775800-674E3BED-5719-4193-B8A8-B8C036014370
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34775800-674E3BED-5719-4193-B8A8-B8C036014370
Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum.
P2860
Q34775800-674E3BED-5719-4193-B8A8-B8C036014370
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34775800-674E3BED-5719-4193-B8A8-B8C036014370
rank
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Statement
wasDerivedFrom
37f769cc93ed668c121abd26b409116c3fab2626
P2860
SPG11 spastic paraplegia. A new cause of juvenile parkinsonism.