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A histopathological and genomics study of the mutated human FAM111B gene related POIKTMP disease

Fibrosis is a pathological feature of many chronic inflammatory diseases, eventually leading to organ failure and death. POIKTMP is a rare, multi-organ fibrosing disease which is associated with mutations of the human FAM111B gene. FAM111B gene codes for a protein whose function is not well characte...

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Bibliographic Details
Main Author: Tambwe, Nadine
Other Authors: Arowolo, Afolake
Format: Thesis
Language:English
Published: Division of General Surgery 2024
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