Clinical manifestations, diagnosis and treatment of Hereditary gelsolin amyloidosis: a case report and systematic review
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https://www.ncbi.nlm.nih.gov/sra/SRP609042
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资源简介：
A 50-year-old female patient presented with proteinuria. Renal tissue biopsy and subsequent mass spectrometry confirmed AGel-type amyloidosis. Genetic testing identified a heterozygous c.487G>A (p.Asp163Asn) mutation in the GSN gene.
创建时间：
2025-08-16
