Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report.

Creator(s)

Stuart M Sprague
Bradley A. Warady, Children's Mercy HospitalFollow

Document Type

Letter to the Editor

Publication Date

7-16-2021

Identifier

DOI: 10.1016/j.xkme.2021.05.005; PMCID: PMC8515063

Journal Title

Kidney Med

Volume

3

Issue

5

First Page

866

Last Page

867

Comments

This article is available under the Creative Commons CC-BY-NC-ND license and permits non-commercial use of the work as published, without adaptation or alteration provided the work is fully attributed.

Publisher's Link: https://www.kidneymedicinejournal.org/article/S2590-0595(21)00158-8/fulltext

Recommended Citation

Sprague SM, Warady BA. Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report. Kidney Med. 2021;3(5):866-867. Published 2021 Jul 16. doi:10.1016/j.xkme.2021.05.005