A Rare Case Of a 2-year-old Boy With Alagille Syndrome and Type 3 Hereditary Hemochromatosis With TFR2 Mutation

Journal article

Peer reviewed

Ammar A. Khayat, Mariko Suchi and Bernadette Vitola

Journal of pediatric gastroenterology and nutrition, Vol.68(4), pp.E68-E70

01/04/2019

PMID: 29985876

Abstract

Gastroenterology & Hepatology

Life Sciences & Biomedicine

Nutrition & Dietetics

Pediatrics

Science & Technology

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Title: A Rare Case Of a 2-year-old Boy With Alagille Syndrome and Type 3 Hereditary Hemochromatosis With TFR2 Mutation
Creators - without role: Ammar A. Khayat - College Station Medical Center
Mariko Suchi - Medical College of Wisconsin
Bernadette Vitola - College Station Medical Center
Publication Details: Journal of pediatric gastroenterology and nutrition, Vol.68(4), pp.E68-E70
Publisher: Lippincott Williams & Wilkins
Number of pages: 3
Identifiers: 9931059808331
Academic Unit: Umm Al Qura University; King Abdulaziz University
Language: English
Resource Type: Journal article