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Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?

Detalles Bibliográficos
Autor principal: Savige, Judy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224634/
https://www.ncbi.nlm.nih.gov/pubmed/30450445
http://dx.doi.org/10.1016/j.ekir.2018.08.002
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author Savige, Judy
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spelling pubmed-62246342018-11-16 Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant? Savige, Judy Kidney Int Rep Editorial Elsevier 2018-08-22 /pmc/articles/PMC6224634/ /pubmed/30450445 http://dx.doi.org/10.1016/j.ekir.2018.08.002 Text en © 2018 International Society of Nephrology. Published by Elsevier Inc. http://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 Editorial
Savige, Judy
Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?
title Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?
title_full Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?
title_fullStr Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?
title_full_unstemmed Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?
title_short Should We Diagnose Autosomal Dominant Alport Syndrome When There Is a Pathogenic Heterozygous COL4A3 or COL4A4 Variant?
title_sort should we diagnose autosomal dominant alport syndrome when there is a pathogenic heterozygous col4a3 or col4a4 variant?
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224634/
https://www.ncbi.nlm.nih.gov/pubmed/30450445
http://dx.doi.org/10.1016/j.ekir.2018.08.002
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