Association of Clinical Phenotypes in Haploinsufficiency A20 (HA20) With Disrupted Domains of A20

Background: Haploinsufficiency A20 (HA20) is a newly described monogenic disease characterized by a wide spectrum of manifestations and caused by heterozygous mutations in TNFAIP3 which encodes A20 protein. TNFAIP3 mutation leads to disruption of the A20 ovarian tumor (OTU) domain and/or the zinc fi...

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Detalles Bibliográficos
Autores principales: Chen, Yu, Ye, Zhenghao, Chen, Liping, Qin, Tingting, Seidler, Ursula, Tian, De'an, Xiao, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546856/
https://www.ncbi.nlm.nih.gov/pubmed/33101300
http://dx.doi.org/10.3389/fimmu.2020.574992

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7546856/
https://www.ncbi.nlm.nih.gov/pubmed/33101300
http://dx.doi.org/10.3389/fimmu.2020.574992

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