A Rare Case Of a 2-year-old Boy With Alagille Syndrome and Type 3 Hereditary Hemochromatosis With TFR2 Mutation. J Pediatr Gastroenterol Nutr 2019 Apr;68(4):e68-e70
Date
07/10/2018Pubmed ID
29985876DOI
10.1097/MPG.0000000000002078Scopus ID
2-s2.0-85063633970 (requires institutional sign-in at Scopus site) 1 CitationAuthor List
Khayat AA, Suchi M, Vitola BAuthors
Mariko Suchi MD, PhD Associate Professor in the Pathology department at Medical College of WisconsinBernadette Vitola MD, MPH Associate Professor in the Pediatrics department at Medical College of Wisconsin
MESH terms used to index this publication - Major topics in bold
Alagille SyndromeHemochromatosis
Humans
Infant
Male
Mutation
Receptors, Transferrin
