Clinical Features and Familial Mutations in an Autosomal-Inherited Alport Syndrome Patient With the Presentation of Nephrotic Syndrome

Background: The aim of this study was to report the clinical features and mutations in a patient with autosomal-inherited Alport syndrome (AS).Methods: We examined the clinical data, mutation analysis results, and family tree of a patient with autosomal-inherited AS, who had nephrotic syndrome as he...

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Hlavní autoři: Dahai Wang (Autor), Chunrong Shan (Autor), Xinxin Jing (Autor), Qiuye Zhang (Autor), Hong Chang (Autor), Yi Lin (Autor)
Médium: Kniha
Vydáno: Frontiers Media S.A., 2021-11-01T00:00:00Z.
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