Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasis.

Hermeziu, Bogdan; Sanlaville, Damien; Girard, Muriel; Léonard, Claude; Lyonnet, Stanislas; Jacquemin, Emmanuel

Hermeziu, Bogdan; Sanlaville, Damien; Girard, Muriel; Léonard, Claude; Lyonnet, Stanislas; Jacquemin, Emmanuel.

Affiliation

Hermeziu B; Pediatric Hepatology, Bicêtre University Hospital, Paris, France.

J Pediatr Gastroenterol Nutr ; 42(1): 114-6, 2006 Jan.

Article in En | MEDLINE | ID: mdl-16385265

Subject(s)

ATP-Binding Cassette Transporters/genetics; Cholestasis/genetics; Genetic Predisposition to Disease; Mutation; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters/metabolism; Cholestasis/congenital; Cholestasis/metabolism; Female; Gene Deletion; Humans; Infant, Newborn; Risk Factors

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Collection: 01-internacional Database: MEDLINE Main subject: Cholestasis / ATP-Binding Cassette Transporters / Genetic Predisposition to Disease / Mutation Type of study: Etiology_studies / Risk_factors_studies Limits: Female / Humans / Newborn Language: En Journal: J Pediatr Gastroenterol Nutr Year: 2006 Document type: Article Affiliation country: France

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