Chinese familial transthyretin amyloidosis with vitreous involvement is associated with the transthyretin mutation Gly83Arg: a case report and literature review
Author:
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/13506129.2014.892871
Reference9 articles.
1. Transthyretin synthesis in rabbit ciliary pigment epithelium
2. Impact of Liver Transplantation on Transthyretin-Related Ocular Amyloidosis in Japanese Patients
3. RECURRENCE OF VITREOUS AMYLOIDOSIS AND NEED OF SURGICAL REINTERVENTION IN PORTUGUESE PATIENTS WITH FAMILIAL AMYLOIDOSIS ATTR V30M
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1. The Gly103Arg variant in hereditary transthyretin amyloidosis;Frontiers in Neurology;2024-09-09
2. Rare manifestation of familial vitreous amyloidosis caused by Gly103Arg transthyretin;International Journal of Ophthalmology;2023-07-18
3. Detection and Diagnosis of Cardiac Amyloidosis in Egypt;Cardiology and Therapy;2023-01-07
4. Case Report: Hereditary transthyretin (ATTRv) amyloidosis: The p.G103R mutation of the transthyretin gene in a Han Chinese family is associated with vitreous hemorrhage;Frontiers in Genetics;2022-09-15
5. Clinical phenotypes and genetic features of hereditary transthyretin amyloidosis patients in China;Orphanet Journal of Rare Diseases;2022-09-02
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