Familial Interstitial Lung Disease Caused by Mutation of the STING1 Gene
Mutations that affect the STING1 (TMEM173) gene cause a rare autoinflammatory syndrome, which is known as STING-associated vasculopathy with onset in infancy (SAVI) and which was initially described in 2014 (1). Thus far, only four reports have been conducted regarding families affected with SAVI in...
Saved in:
Main Authors: | Jinying Li (Author), Shuhua An (Author), Zhongdong Du (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2020-09-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Potential of resveratrol in the treatment of interstitial lung disease
by: Rongxiu Huo, et al.
Published: (2023) -
New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene
by: Imen Rejeb, et al.
Published: (2021) -
Case report: Fibrotic interstitial lung disease as the initial manifestation of hereditary pulmonary alveolar proteinosis caused by CSF2RB mutation
by: Qiuhong Li, et al.
Published: (2024) -
A rare cause of interstitial lung disease with skin lesion
by: Smera Ramakrishnan, et al.
Published: (2022) -
Interstitial Lung Diseases
Published: (2019)