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Q36317330-92568CF5-3C3D-400F-9A6B-AAEE2D64A745
Q36317330-92568CF5-3C3D-400F-9A6B-AAEE2D64A745
BestRank
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http://www.wikidata.org/entity/statement/Q36317330-92568CF5-3C3D-400F-9A6B-AAEE2D64A745
NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup.
P2860
Q36317330-92568CF5-3C3D-400F-9A6B-AAEE2D64A745
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36317330-92568CF5-3C3D-400F-9A6B-AAEE2D64A745
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wasDerivedFrom
f1bb0aa4e66ed64b98c335ffaf914b5993394e68
P2860
Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54).