Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis

Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis

Abstract Background Focal and segmental glomerulosclerosis (FSGS) is a histological pathology that characterizes a wide spectrum of diseases. Many genes associated with FSGS have been studied previously, but there are still some FSGS families reported in the literature without the identification of...

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Main Authors: Hafiz Muhammad Jafar Hussain, Yikai Cai, Qinjie Weng, Jun Tong, Ayesha Aftab, Yuanmeng Jin, Jian Liu, Shuwen Yu, Zhengying Fang, Wen Du, Xiaoxia Pan, Hong Ren, Jingyuan Xie
Format: Article
Language:English
Published: BMC 2022-11-01
Series:Human Genomics
Subjects:
FSGS
Whole-exome sequencing
XPO5 gene
Adult-onset
Autosomal
Dominant
Online Access:https://doi.org/10.1186/s40246-022-00430-y

Internet

https://doi.org/10.1186/s40246-022-00430-y

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