Fainting Fanconi syndrome clarified by proxy: a case report.

2.50
Hdl Handle:
http://hdl.handle.net/11287/620412
Title:
Fainting Fanconi syndrome clarified by proxy: a case report.
Authors:
Walsh, S. B.; Unwin, R.; Kleta, R.; Van't Hoff, W.; Bass, P.; Hussain, K.; Ellard, Sian ( 0000-0002-7620-5526 ) ; Bockenhauer, D.
Abstract:
Rare diseases may elude diagnosis due to unfamiliarity of the treating physicians with the specific disorder. Yet, advances in genetics have tremendously enhanced our ability to establish specific and sometimes surprising diagnoses.
Citation:
Fainting Fanconi syndrome clarified by proxy: a case report. 2017, 18 (1):230 BMC Nephrol
Publisher:
BioMed Central
Journal:
BMC Nephrology
Issue Date:
11-Jul-2017
URI:
http://hdl.handle.net/11287/620412
DOI:
10.1186/s12882-017-0649-8
PubMed ID:
28693455
Additional Links:
https://bmcnephrol.biomedcentral.com/articles/10.1186/s12882-017-0649-8
Note:
This article is freely available via Open Access. Click on the Additional Link above to access the full-text via the publisher's site.
Type:
Journal Article; Case Report
Language:
en
ISSN:
1471-2369
Appears in Collections:
Molecular Genetics; 2017 RD&E publications

Full metadata record

DC FieldValue Language
dc.contributor.authorWalsh, S. B.en
dc.contributor.authorUnwin, R.en
dc.contributor.authorKleta, R.en
dc.contributor.authorVan't Hoff, W.en
dc.contributor.authorBass, P.en
dc.contributor.authorHussain, K.en
dc.contributor.authorEllard, Sianen
dc.contributor.authorBockenhauer, D.en
dc.date.accessioned2017-09-19T13:27:18Z-
dc.date.available2017-09-19T13:27:18Z-
dc.date.issued2017-07-11-
dc.identifier.citationFainting Fanconi syndrome clarified by proxy: a case report. 2017, 18 (1):230 BMC Nephrolen
dc.identifier.issn1471-2369-
dc.identifier.pmid28693455-
dc.identifier.doi10.1186/s12882-017-0649-8-
dc.identifier.urihttp://hdl.handle.net/11287/620412-
dc.description.abstractRare diseases may elude diagnosis due to unfamiliarity of the treating physicians with the specific disorder. Yet, advances in genetics have tremendously enhanced our ability to establish specific and sometimes surprising diagnoses.en
dc.language.isoenen
dc.publisherBioMed Centralen
dc.relation.urlhttps://bmcnephrol.biomedcentral.com/articles/10.1186/s12882-017-0649-8en
dc.rightsArchived with thanks to BMC nephrology. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.titleFainting Fanconi syndrome clarified by proxy: a case report.en
dc.typeJournal Articleen
dc.typeCase Reporten
dc.identifier.journalBMC Nephrologyen
dc.description.noteThis article is freely available via Open Access. Click on the Additional Link above to access the full-text via the publisher's site.en
dc.type.versionPublisheden

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