Sodium taurocholate co-transporting polypeptide deficiency.

Schneider, A L; Köhler, H; Röthlisberger, B; Grobholz, R; McLin, V A

Schneider, A L; Köhler, H; Röthlisberger, B; Grobholz, R; McLin, V A.

Affiliation

Schneider AL; Swiss Pediatric Liver Center, Division of Pediatric Specialties, Department of Pediatrics, Gynecology and Obstetrics, University of Geneva, Geneva, Switzerland. Electronic address: anais.schneider@protonmail.com.
Köhler H; Department of Pediatrics, Hospital of Aarau, Switzerland.
Röthlisberger B; Laboratory for human genetic testing and genetic counselling, Zurich.
Grobholz R; Department of Pathology, Hospital of Aarau, Switzerland.
McLin VA; Swiss Pediatric Liver Center, Division of Pediatric Specialties, Department of Pediatrics, Gynecology and Obstetrics, University of Geneva, Geneva, Switzerland.

Clin Res Hepatol Gastroenterol ; 46(3): 101824, 2022 03.

Article de En | MEDLINE | ID: mdl-34757153

Sujet(s)
Mots clés

Failure to thrive; Hypercholanemia; NTCP deficiency

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Acide taurocholique / Symporteurs Type d'étude: Etiology_studies / Prognostic_studies Limites: Adolescent / Child, preschool / Female / Humans / Newborn Langue: En Journal: Clin Res Hepatol Gastroenterol Année: 2022 Type de document: Article Pays de publication: France

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