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Eur J Hum Genet 2012 Feb 29.
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Multiple functions of microsomal triglyceride transfer protein. [Journal Article]
Nutr Metab (Lond) 2012.:14.
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Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia. [Journal Article]
J Lipid Res 2012 Mar; 53(3):548-55.
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Novel mutations in microsomal triglyceride transfer protein including maternal uniparental disomy in two patients with abetalipoproteinemia. [JOURNAL ARTICLE]
Clin Genet 2011 Dec 9.
Full Citation | Publisher Full Text | Find Related Articles | | Okada T, Miyashita M, Fukuhara J, et al.
Anderson's disease/chylomicron retention disease in a Japanese patient with uniparental disomy 7 and a normal SAR1B gene protein coding sequence. [Journal Article, Research Support, Non-U.S. Gov't]
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Neuroacanthocytosis syndromes. [Journal Article, Review]
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Ataxia with vitamin E deficiency and abetalipoproteinemia. [Historical Article, Journal Article, Review]
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The diagnosis and outcomes of persistent diarrhea in infants aged 0-24 months--a Turkish cohort study. [Journal Article]
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Red cells in abetalipoproteinemia. [Comment, Letter]
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