Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II

Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II

Bibliographic Details
Main Authors: Aziz Eghbali, Farzaneh Rahmani, Zahra Aryan, Arndt Borkhardt, Parin Tanzifi, Samaneh Zoghi, Nima Rezaei
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2018-11-01
Series:Acta Medica Iranica
Subjects:
No keywords###
Online Access:https://acta.tums.ac.ir/index.php/acta/article/view/6681
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spelling doaj-ba8ec2ea7d464926b2d424c8a1dba57d2020-11-25T03:35:01ZengTehran University of Medical SciencesActa Medica Iranica0044-60251735-96942018-11-015686681Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type IIAziz Eghbali0Farzaneh Rahmani1Zahra Aryan2Arndt Borkhardt3Parin Tanzifi4Samaneh Zoghi5Nima Rezaei6Department of Pediatric Hematology and Oncology, Arak University of Medical Sciences, Arak, Iran.Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran. AND Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Boston, MA, USA.Pediatric Oncology, Hematology and Clinical Immunology, School of Medicine, Heinrich Heine University, Düsseldorf, Germany.Department of Pathology, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran.CeMM Research Centre for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria. AND Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Vienna, Austria.Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran. AND Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. AND Primary Immunodeficiency Diseases Network (PIDNet), Universal Scientific Education and Research Network (USERN), Tehran, Iran.https://acta.tums.ac.ir/index.php/acta/article/view/6681No keywords###
collection DOAJ
language English
format Article
sources DOAJ
author Aziz Eghbali
Farzaneh Rahmani
Zahra Aryan
Arndt Borkhardt
Parin Tanzifi
Samaneh Zoghi
Nima Rezaei
spellingShingle Aziz Eghbali
Farzaneh Rahmani
Zahra Aryan
Arndt Borkhardt
Parin Tanzifi
Samaneh Zoghi
Nima Rezaei
Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II
Acta Medica Iranica
No keywords###
author_facet Aziz Eghbali
Farzaneh Rahmani
Zahra Aryan
Arndt Borkhardt
Parin Tanzifi
Samaneh Zoghi
Nima Rezaei
author_sort Aziz Eghbali
title Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II
title_short Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II
title_full Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II
title_fullStr Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II
title_full_unstemmed Non-Pathogenic Heterozygous Polymorphism in RAB27A Gene in a Case Suspicious to Griscelli Syndrome, Type II
title_sort non-pathogenic heterozygous polymorphism in rab27a gene in a case suspicious to griscelli syndrome, type ii
publisher Tehran University of Medical Sciences
series Acta Medica Iranica
issn 0044-6025
1735-9694
publishDate 2018-11-01
topic No keywords###
url https://acta.tums.ac.ir/index.php/acta/article/view/6681
work_keys_str_mv AT azizeghbali nonpathogenicheterozygouspolymorphisminrab27ageneinacasesuspicioustogriscellisyndrometypeii
AT farzanehrahmani nonpathogenicheterozygouspolymorphisminrab27ageneinacasesuspicioustogriscellisyndrometypeii
AT zahraaryan nonpathogenicheterozygouspolymorphisminrab27ageneinacasesuspicioustogriscellisyndrometypeii
AT arndtborkhardt nonpathogenicheterozygouspolymorphisminrab27ageneinacasesuspicioustogriscellisyndrometypeii
AT parintanzifi nonpathogenicheterozygouspolymorphisminrab27ageneinacasesuspicioustogriscellisyndrometypeii
AT samanehzoghi nonpathogenicheterozygouspolymorphisminrab27ageneinacasesuspicioustogriscellisyndrometypeii
AT nimarezaei nonpathogenicheterozygouspolymorphisminrab27ageneinacasesuspicioustogriscellisyndrometypeii
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