Phenotypic variation in familial chilblain lupus (FCL) and Aicardi-Goutières syndrome (AGS) associated with <it>TREX1</it> mutation in 4 family members
Saved in:
Main Authors: | Ryder Clive (Author), Davis Penny (Author), Crow Yanick (Author), Taibjee Saleem (Author), Glanville James (Author), Southwood Taunton (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2011-09-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Familial chilblain lupus due to a novel mutation in TREX1 associated with Aicardi-Goutie'res syndrome
by: Cuili Yi, et al.
Published: (2020) -
Clinical heterogeneity among a three-generation Japanese family with D18N <it>TREX1</it> mutation for Aicardi-Goutières syndrome / familial chilblain lupus
by: Heike T, et al.
Published: (2011) -
A case of Aicardi-Goutières syndrome caused by TREX1 gene mutation
by: Zheng Chenhan, et al.
Published: (2023) -
Case Report: Aicardi-Goutières Syndrome Caused by Novel TREX1 Variants
by: De Wu, et al.
Published: (2021) -
Aicardi-Goutieres Syndrome
by: J Gordon Millichap
Published: (1999)