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Q37741094-E8E59C34-05F5-42AF-B79B-8EC1D8889C8A
Q37741094-E8E59C34-05F5-42AF-B79B-8EC1D8889C8A
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http://www.wikidata.org/entity/statement/Q37741094-E8E59C34-05F5-42AF-B79B-8EC1D8889C8A
Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation.
P2860
Q37741094-E8E59C34-05F5-42AF-B79B-8EC1D8889C8A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37741094-E8E59C34-05F5-42AF-B79B-8EC1D8889C8A
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wasDerivedFrom
34a1df22ce1c29be8e9b9ca2d4f44b8f498842e1
P2860
Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54).