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

10.1002/pro.2265

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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
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Institution:	National University of Singapore

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spelling	sg-nus-scholar.10635-1552802024-11-11T07:42:09Z Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients An, O Gursoy, A Gurgey, A Keskin, O CANCER SCIENCE INSTITUTE OF SINGAPORE Dr Omer An 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 10.1002/pro.2265 Protein Science 22 6 823-839 2019-06-07T01:36:32Z 2019-06-07T01:36:32Z 2013-06-01 2019-06-03T09:41:09Z Article An, O, Gursoy, A, Gurgey, A, Keskin, O (2013-06-01). Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients. Protein Science 22 (6) : 823-839. ScholarBank@NUS Repository. https://doi.org/10.1002/pro.2265 0961-8368 1469-896X https://scholarbank.nus.edu.sg/handle/10635/155280 Wiley Elements
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	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
spellingShingle	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 An, O Gursoy, A Gurgey, A Keskin, O Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients
description	10.1002/pro.2265
author2	CANCER SCIENCE INSTITUTE OF SINGAPORE
author_facet	CANCER SCIENCE INSTITUTE OF SINGAPORE An, O Gursoy, A Gurgey, A Keskin, O
format	Article
author	An, O Gursoy, A Gurgey, A Keskin, O
author_sort	An, O
title	Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients
title_short	Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients
title_full	Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients
title_fullStr	Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients
title_full_unstemmed	Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients
title_sort	structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (fhl2) patients
publisher	Wiley
publishDate	2019
url	https://scholarbank.nus.edu.sg/handle/10635/155280
_version_	1821188826237763584

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

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