Hereditary Gelsolin Amyloidosis: A New Japanese Case with Cutis Laxa as a Diagnostic Clue
Author:
Publisher
Medical Journals Sweden AB
Subject
Dermatology,General Medicine
Cited by 7 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. GSNgene frameshift mutations in Alzheimer’s disease;Journal of Neurology, Neurosurgery & Psychiatry;2023-01-17
2. Analyses Mutations in GSN, CST3, TTR, and ITM2B Genes in Chinese Patients With Alzheimer’s Disease;Frontiers in Aging Neuroscience;2020-09-10
3. Histoproteomic Characterization of Localized Cutaneous Amyloidosis in X-Linked Reticulate Pigmentary Disorder;Skin Pharmacology and Physiology;2017
4. In vivo skin biophysical behaviour and surface topography as a function of ageing;Journal of the Mechanical Behavior of Biomedical Materials;2013-12
5. Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases;Clinical Kidney Journal;2013-03-27
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