Identification of new α-galactosidase A mutation responsible for Fabry disease: A case report-Reference-Cited by-同舟云学术

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Identification of new α-galactosidase A mutation responsible for Fabry disease: A case report

Published:2019-02-01 Issue:2 Volume:91 Page:126-128
ISSN:0301-0430
Container-title:Clinical Nephrology
language:en
Short-container-title:CN

Author:

Battaglia Yuri,Scalia Simone,Rinaldi Rosa,Storari Alda,Mignani Renzo,Russo Domenico,Duro Giovanni

Publisher

Dustri-Verlgag Dr. Karl Feistle

Subject

Nephrology,General Medicine

Cited by 3 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. Dapaglifozin on Albuminuria in Chronic Kidney Disease Patients with FabrY Disease: The DEFY Study Design and Protocol;Journal of Clinical Medicine;2023-05-26

2. Deficiency in the Screening Process of Fabry Disease: Analysis of Chronic Kidney Patients Not on Dialysis;Frontiers in Medicine;2021-02-09

3. Genotype–Phenotype Correlation in a New Fabry-Disease-Causing Mutation;Medicina;2019-05-07

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