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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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| Publicado no: | Clin Pediatr Endocrinol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Japanese Society for Pediatric Endocrinology
2019
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| Assuntos: | |
| Acesso em linha: | 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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