Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation

Detalles Bibliográficos
Autores principales: Singh, Prince, Chebib, Fouad T., Cogal, Andrea G., Gavrilov, Dimitar K., Harris, Peter C., Lieske, John C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Nephrology Round
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270974/
https://www.ncbi.nlm.nih.gov/pubmed/32518881
http://dx.doi.org/10.1016/j.ekir.2020.04.004
_version_ 1783541999783116800
author Singh, Prince
Chebib, Fouad T.
Cogal, Andrea G.
Gavrilov, Dimitar K.
Harris, Peter C.
Lieske, John C.
author_facet Singh, Prince
Chebib, Fouad T.
Cogal, Andrea G.
Gavrilov, Dimitar K.
Harris, Peter C.
Lieske, John C.
author_sort Singh, Prince
collection PubMed
description
format Online
Article
Text
id pubmed-7270974
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-72709742020-06-08 Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation Singh, Prince Chebib, Fouad T. Cogal, Andrea G. Gavrilov, Dimitar K. Harris, Peter C. Lieske, John C. Kidney Int Rep Nephrology Round Elsevier 2020-04-13 /pmc/articles/PMC7270974/ /pubmed/32518881 http://dx.doi.org/10.1016/j.ekir.2020.04.004 Text en © 2020 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 Nephrology Round
Singh, Prince
Chebib, Fouad T.
Cogal, Andrea G.
Gavrilov, Dimitar K.
Harris, Peter C.
Lieske, John C.
Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation
title Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation
title_full Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation
title_fullStr Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation
title_full_unstemmed Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation
title_short Pyridoxine Responsiveness in a Type 1 Primary Hyperoxaluria Patient With a Rare (Atypical) AGXT Gene Mutation
title_sort pyridoxine responsiveness in a type 1 primary hyperoxaluria patient with a rare (atypical) agxt gene mutation
topic Nephrology Round
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270974/
https://www.ncbi.nlm.nih.gov/pubmed/32518881
http://dx.doi.org/10.1016/j.ekir.2020.04.004
work_keys_str_mv AT singhprince pyridoxineresponsivenessinatype1primaryhyperoxaluriapatientwitharareatypicalagxtgenemutation
AT chebibfouadt pyridoxineresponsivenessinatype1primaryhyperoxaluriapatientwitharareatypicalagxtgenemutation
AT cogalandreag pyridoxineresponsivenessinatype1primaryhyperoxaluriapatientwitharareatypicalagxtgenemutation
AT gavrilovdimitark pyridoxineresponsivenessinatype1primaryhyperoxaluriapatientwitharareatypicalagxtgenemutation
AT harrispeterc pyridoxineresponsivenessinatype1primaryhyperoxaluriapatientwitharareatypicalagxtgenemutation
AT lieskejohnc pyridoxineresponsivenessinatype1primaryhyperoxaluriapatientwitharareatypicalagxtgenemutation

Ejemplares similares