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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

07/10/2018

Pubmed ID

29985876

DOI

10.1097/MPG.0000000000002078

Scopus ID

2-s2.0-85063633970

Author List

Khayat AA, Suchi M, Vitola B

Authors

Mariko Suchi MD, PhD Associate Professor in the Pathology department at Medical College of Wisconsin
Bernadette Vitola MD Associate Professor in the Pediatrics department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Alagille Syndrome
Hemochromatosis
Hispanic Americans
Humans
Infant
Male
Mutation
Receptors, Transferrin
jenkins-FCD Prod-482 91ad8a360b6da540234915ea01ff80e38bfdb40a