Familial Primary Localized Cutaneous Amyloidosis Results from Either Dominant or Recessive Mutations in OSMR
Author:
Publisher
Medical Journals Sweden AB
Subject
Dermatology,General Medicine
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Thyroid Malignancy and Cutaneous Lichen Amyloidosis: Key Points Amid RET Pathogenic Variants in Medullary Thyroid Cancer/Multiple Endocrine Neoplasia Type 2 (MEN2);International Journal of Molecular Sciences;2024-09-10
2. Primary Localized Cutaneous Amyloidosis in Central Europe: A Retrospective Monocentric Study on Epidemiology and Therapy;Journal of Clinical Medicine;2023-12-14
3. Identification of polymorphic loci in OSMR and GHR genes and analysis of their association with growth traits in sheep;Animal Biotechnology;2022-08-01
4. LC‐MS/MS and immuno‐electron subtyping combined with genetics show that OSMR mutations cause amyloid deposition of keratins 5/14 in familial primary localized cutaneous amyloidosis;Journal of the European Academy of Dermatology and Venereology;2021-09-17
5. Primary Localized Cutaneous Amyloidosis of Keratinocyte Origin: An Update with Emphasis on Atypical Clinical Variants;American Journal of Clinical Dermatology;2021-07-21
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