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Article: ADPKD Progression in Patients With No Apparent Family History and No Mutation Detected by Sanger Sequencing

TitleADPKD Progression in Patients With No Apparent Family History and No Mutation Detected by Sanger Sequencing
Authors
Braun, William E.Abebe, Kaleab Z.Brosnahan, GodelaPatterson, Charity G.Chapman, Arlene B.Harris, Peter C.Hogan, Marie C.Perrone, Ronald D.Torres, Vicente E.Miskulin, Dana C.Steinman, Theodore I.Winklhofer, Franz T.Rahbari-Oskoui, Frederic F.Czarnecki, Peter G.Bae, Kyongtae T.Grantham, Jared J.Flessner, Michael F.Schrier, Robert W.
Issue Date2018
Citation
American Journal of Kidney Diseases, 2018, v. 71, n. 2, p. 294-296 How to Cite?
DOI: http://dx.doi.org/10.1053/j.ajkd.2017.09.008
Persistent Identifierhttp://hdl.handle.net/10722/316161
ISSN
0272-6386
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.096
ISI Accession Number ID
WOS:000423670500026

 

DC FieldValueLanguage
dc.contributor.authorBraun, William E.-
dc.contributor.authorAbebe, Kaleab Z.-
dc.contributor.authorBrosnahan, Godela-
dc.contributor.authorPatterson, Charity G.-
dc.contributor.authorChapman, Arlene B.-
dc.contributor.authorHarris, Peter C.-
dc.contributor.authorHogan, Marie C.-
dc.contributor.authorPerrone, Ronald D.-
dc.contributor.authorTorres, Vicente E.-
dc.contributor.authorMiskulin, Dana C.-
dc.contributor.authorSteinman, Theodore I.-
dc.contributor.authorWinklhofer, Franz T.-
dc.contributor.authorRahbari-Oskoui, Frederic F.-
dc.contributor.authorCzarnecki, Peter G.-
dc.contributor.authorBae, Kyongtae T.-
dc.contributor.authorGrantham, Jared J.-
dc.contributor.authorFlessner, Michael F.-
dc.contributor.authorSchrier, Robert W.-
dc.date.accessioned2022-08-24T15:49:27Z-
dc.date.available2022-08-24T15:49:27Z-
dc.date.issued2018-
dc.identifier.citationAmerican Journal of Kidney Diseases, 2018, v. 71, n. 2, p. 294-296-
dc.identifier.issn0272-6386-
dc.identifier.urihttp://hdl.handle.net/10722/316161-
dc.languageeng-
dc.relation.ispartofAmerican Journal of Kidney Diseases-
dc.titleADPKD Progression in Patients With No Apparent Family History and No Mutation Detected by Sanger Sequencing-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1053/j.ajkd.2017.09.008-
dc.identifier.pmid29203126-
dc.identifier.scopuseid_2-s2.0-85035329155-
dc.identifier.volume71-
dc.identifier.issue2-
dc.identifier.spage294-
dc.identifier.epage296-
dc.identifier.eissn1523-6838-
dc.identifier.isiWOS:000423670500026-

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