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

Detalles Bibliográficos
Autores principales: Sprague, Stuart M., Warady, Bradley A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515063/
https://www.ncbi.nlm.nih.gov/pubmed/34693267
http://dx.doi.org/10.1016/j.xkme.2021.05.005
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author Sprague, Stuart M.
Warady, Bradley A.
author_facet Sprague, Stuart M.
Warady, Bradley A.
author_sort Sprague, Stuart M.
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spelling pubmed-85150632021-10-21 Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report Sprague, Stuart M. Warady, Bradley A. Kidney Med Correspondence Elsevier 2021-07-16 /pmc/articles/PMC8515063/ /pubmed/34693267 http://dx.doi.org/10.1016/j.xkme.2021.05.005 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Correspondence
Sprague, Stuart M.
Warady, Bradley A.
Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report
title Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report
title_full Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report
title_fullStr Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report
title_full_unstemmed Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report
title_short Family Genetic Screening to Identify Cases of Alport Syndrome: A Case Study Report
title_sort family genetic screening to identify cases of alport syndrome: a case study report
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515063/
https://www.ncbi.nlm.nih.gov/pubmed/34693267
http://dx.doi.org/10.1016/j.xkme.2021.05.005
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