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Q34308654-BDFB28D6-3D84-4DE2-9460-C3BA7E914192
Q34308654-BDFB28D6-3D84-4DE2-9460-C3BA7E914192
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34308654-BDFB28D6-3D84-4DE2-9460-C3BA7E914192
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.
P2860
Q34308654-BDFB28D6-3D84-4DE2-9460-C3BA7E914192
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34308654-BDFB28D6-3D84-4DE2-9460-C3BA7E914192
rank
NormalRank
type
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Statement
wasDerivedFrom
2aba3682e682731370174e8d415b938ad4548c25
P2860
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families.