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Q35041284-5EA4A87C-CE43-4A98-AB5F-AA52D444066D
Q35041284-5EA4A87C-CE43-4A98-AB5F-AA52D444066D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35041284-5EA4A87C-CE43-4A98-AB5F-AA52D444066D
State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis.
P2860
Q35041284-5EA4A87C-CE43-4A98-AB5F-AA52D444066D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35041284-5EA4A87C-CE43-4A98-AB5F-AA52D444066D
rank
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wasDerivedFrom
f1fd6ee657fe488c4d3c011b2958edcb221ab9ea
P2860
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.