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Article

Neonatal cholestatic liver disease in an Asian patient with a homozygous mutation in the oxysterol 7alpha-hydroxylase gene.

Journal of pediatric gastroenterology and nutrition - 1 Apr 2008

Ueki Isao, Kimura Akihiko, Nishiyori Atsushi, Chen Huey-Ling, Takei Hajime, Nittono Hiroshi, Kurosawa Takao

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Share to Bile Acids and Salts
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 18367963
DOI: 10.1097/MPG.0b013e31815a9911

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Related research

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Neonatal cholestatic liver disease in an Asian patient with a homozygous mutation in the oxysterol 7alpha-hydroxylase gene.PMID 18367963Read ↗

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Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease.Semantic proximity Read ↗

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Disruption of cholesterol 7alpha-hydroxylase gene in mice. II. Bile acid deficiency is overcome by induction of oxysterol 7alpha-hydroxylase.Semantic proximity Read ↗

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