A TYK2 Gene Mutation c.2395G>A Leads to TYK2 Deficiency: A Case Report and Literature Review

Tyrosine kinase 2 (TYK2) deficiency was formerly defined in patients suffering from autosomal recessive hyperimmunoglobulin E syndrome (AR-HIES). In recent years, it was proposed that human TYK2 deficiency is probably not a common cause of the AR-HIES but a distinctive illness object. In the current...

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Detalles Bibliográficos
Autores principales: Wu, Peilin, Chen, Suqing, Wu, Bin, Chen, Junhong, Lv, Ge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267021/
https://www.ncbi.nlm.nih.gov/pubmed/32537443
http://dx.doi.org/10.3389/fped.2020.00253

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267021/
https://www.ncbi.nlm.nih.gov/pubmed/32537443
http://dx.doi.org/10.3389/fped.2020.00253

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