1999
DOI: 10.1007/s004150050499
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Familial ataxia with isolated vitamin E deficiency not due to mutation of à-TTP

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Cited by 4 publications
(1 citation statement)
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“…In contrast to a high affinity to α-tocopherol (100%), α-tocopherol transfer protein (α-TTP) has a much lower affinity towards other vitamin E forms; 50%, 10-30%, and 1% affinity to β-tocopherol, γ-tocopherol, and δ-tocopherol, respectively [78], and plays an important role in the maintenance of high concentrations of α-tocopherol in plasma and some tissues [79,80]. A reduction in plasma γ-tocopherol during enhanced intake of α-tocopherol, such as through supplemental intake, can be explained by the more rapid metabolism of γ-tocopherol occurring when α-tocopherol intake is increased [81].…”
Section: Discussionmentioning
confidence: 99%
“…In contrast to a high affinity to α-tocopherol (100%), α-tocopherol transfer protein (α-TTP) has a much lower affinity towards other vitamin E forms; 50%, 10-30%, and 1% affinity to β-tocopherol, γ-tocopherol, and δ-tocopherol, respectively [78], and plays an important role in the maintenance of high concentrations of α-tocopherol in plasma and some tissues [79,80]. A reduction in plasma γ-tocopherol during enhanced intake of α-tocopherol, such as through supplemental intake, can be explained by the more rapid metabolism of γ-tocopherol occurring when α-tocopherol intake is increased [81].…”
Section: Discussionmentioning
confidence: 99%