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Q50299507-D838599B-F20F-4B0C-B53D-A895458DD121
Q50299507-D838599B-F20F-4B0C-B53D-A895458DD121
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50299507-D838599B-F20F-4B0C-B53D-A895458DD121
GLS loss of function causes autosomal recessive spastic ataxia and optic atrophy.
P2860
Q50299507-D838599B-F20F-4B0C-B53D-A895458DD121
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50299507-D838599B-F20F-4B0C-B53D-A895458DD121
rank
NormalRank
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Statement
wasDerivedFrom
fae29d5e52380f7abec0efb08a401b9a436710c7
P2860
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia