Autosomal dominant Hashimoto’s thyroiditis with a mutation in TNFAIP3

Hashimoto’s thyroiditis (HT) is an autoimmune disease thought to involve a combination of genetic and environmental factors, but its detailed pathogenesis is unknown. We present a family with haploinsufficiency of the gene encoding tumor necrosis factor α-induced protein 3 (TNFAIP3, also known as A2...

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Bibliografiska uppgifter
I publikationen:Clin Pediatr Endocrinol
Huvudupphovsmän: Hori, Tomohiro, Ohnishi, Hidenori, Kadowaki, Tomonori, Kawamoto, Norio, Matsumoto, Hideki, Ohara, Osamu, Fukao, Toshiyuki
Materialtyp: Artigo
Språk:Inglês
Publicerad: The Japanese Society for Pediatric Endocrinology 2019
Ämnen:
Case Report
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6646238/
https://ncbi.nlm.nih.gov/pubmed/31384100
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.28.91
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