The α-tocopherol transfer protein is essential for vertebrate embryogenesis.

The hepatic α-tocopherol transfer protein (TTP) is required for optimal α-tocopherol bioavailability in humans; mutations in the human TTPA gene result in the heritable disorder ataxia with vitamin E deficiency (AVED, OMIM #277460). TTP is also expressed in mammalian uterine and placental cells and...

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Bibliographic Details
Main Authors: Galen W Miller, Lynn Ulatowski, Edwin M Labut, Katie M Lebold, Danny Manor, Jeffrey Atkinson, Carrie L Barton, Robert L Tanguay, Maret G Traber
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0047402&type=printable