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CARD9mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficiencies

[...]including indels, 1333 variants involving 1000 different genes and 1220 variants involving 943 different genes were detected in patient 1 and patient 2, respectively. All these detected mutations were not found in 220 ethnically matched control subjects. [...]CARD9 was selected as the most like... Full description

Journal Title: Journal of allergy and clinical immunology 2014-03-01, Vol.133 (3), p.905
Main Author: Xiaowen Wang
Other Authors: Wenyan Wang , Zhimiao Lin , Xiaolin Wang , Ting Li , Jin Yu , Wei Liu , Zhongsheng Tong , Yonghao Xu , Junling Zhang , Liping Guan , Lanlan Dai , Yong Yang , Wenling Han , Ruoyu Li
Format: Electronic Article Electronic Article
Language: English
Subjects:
Quelle: Alma/SFX Local Collection
Publisher: St. Louis: Elsevier Limited
ID: ISSN: 0091-6749
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recordid: cdi_proquest_journals_1644784489
title: CARD9mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficiencies
format: Article
creator:
  • Xiaowen Wang
  • Wenyan Wang
  • Zhimiao Lin
  • Xiaolin Wang
  • Ting Li
  • Jin Yu
  • Wei Liu
  • Zhongsheng Tong
  • Yonghao Xu
  • Junling Zhang
  • Liping Guan
  • Lanlan Dai
  • Yong Yang
  • Wenling Han
  • Ruoyu Li
subjects:
  • Cytokines
  • Families & family life
  • Fungal infections
  • Fungi
  • Haplotypes
  • Mutation
  • Patients
  • Yeast
ispartof: Journal of allergy and clinical immunology, 2014-03-01, Vol.133 (3), p.905
description: [...]including indels, 1333 variants involving 1000 different genes and 1220 variants involving 943 different genes were detected in patient 1 and patient 2, respectively. All these detected mutations were not found in 220 ethnically matched control subjects. [...]CARD9 was selected as the most likely causative gene underlying phaeohyphomycosis in these patients.
language: eng
source: Alma/SFX Local Collection
identifier: ISSN: 0091-6749
fulltext: fulltext
issn:
  • 0091-6749
  • 1097-6825
url: Link


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titleCARD9mutations linked to subcutaneous phaeohyphomycosis and TH17 cell deficiencies
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creatorXiaowen Wang ; Wenyan Wang ; Zhimiao Lin ; Xiaolin Wang ; Ting Li ; Jin Yu ; Wei Liu ; Zhongsheng Tong ; Yonghao Xu ; Junling Zhang ; Liping Guan ; Lanlan Dai ; Yong Yang ; Wenling Han ; Ruoyu Li
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description[...]including indels, 1333 variants involving 1000 different genes and 1220 variants involving 943 different genes were detected in patient 1 and patient 2, respectively. All these detected mutations were not found in 220 ethnically matched control subjects. [...]CARD9 was selected as the most likely causative gene underlying phaeohyphomycosis in these patients.
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abstract[...]including indels, 1333 variants involving 1000 different genes and 1220 variants involving 943 different genes were detected in patient 1 and patient 2, respectively. All these detected mutations were not found in 220 ethnically matched control subjects. [...]CARD9 was selected as the most likely causative gene underlying phaeohyphomycosis in these patients.
copSt. Louis
pubElsevier Limited
doi10.1016/j.jaci.2013.09.033