Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients

Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients

10.1002/pro.2265

Saved in:
Bibliographic Details
Main Authors: An, O, Gursoy, A, Gurgey, A, Keskin, O
Other Authors: CANCER SCIENCE INSTITUTE OF SINGAPORE
Format: Article
Published: Wiley 2019
Subjects:
Adolescent
Adult
Child
Child, Preschool
Female
Humans
Infant
Infant, Newborn
Lymphohistiocytosis, Hemophagocytic
Male
Models, Molecular
Mutation, Missense
Perforin
Polymorphism, Single Nucleotide
Protein Conformation
Young Adult
Online Access:https://scholarbank.nus.edu.sg/handle/10635/155280
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: National University of Singapore
Description
Summary:10.1002/pro.2265

Similar Items