Associated Papers
Association of rare variants in genes of immune regulation with pediatric autoimmune CNS diseases.
Jafarpour S et al.
Journal of Neurology, 2022
Novel Mutations in ACP5 and SAMHD1 in a Patient With Pediatric Systemic Lupus Erythematosus.
Hong SM et al.
Frontiers in Pediatrics, 2022
Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey.
Briggs TA et al.
Journal of Clinical Immunology, 2016
Severe immune dysregulation with neurological impairment and minor bone changes in a child with spondyloenchondrodysplasia due to two novel mutations in the ACP5 gene.
Girschick H et al.
Pediatric Rheumatology Online Journal, 2015
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