Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome

Almenn færsla
dc.contributor.authorAradottir, Sigridur Sunna
dc.contributor.authorKristoffersson, Ann-Charlotte
dc.contributor.authorJensson, Brynjar O
dc.contributor.authorSulem, Patrick
dc.contributor.authorGong, Henning
dc.contributor.authorPálsson, Runólfur
dc.contributor.authorKarpman, Diana
dc.contributor.departmentFaculty of Medicine
dc.date.accessioned2025-11-20T09:15:17Z
dc.date.available2025-11-20T09:15:17Z
dc.date.issued2023-05
dc.descriptionFunding Information: The authors acknowledge scientific discussions with Professor Nancy Segal, California State University Fullerton. We are grateful for bioinformatic expertise provided by Dr. Petter Storm, Lund University. We thank Dr. Ida Arvidsson, Dr. Annie Willysson, and Dr. Ashmita Tontanahal of the Department of Pediatrics, Lund University for their help with microscopy and quantification. This paper was presented in poster form at the 18th European Meeting on Complement in Human Disease 26-29/8, 2022 in Bern Switzerland. The authors are grateful to the patients and their family members for participating in the study. The Swedish Research Council (2020-02200, 2017-01920), The Knut and Alice Wallenberg Foundation (Wallenberg Clinical Scholar 2015.0320), Skåne Centre of Excellence in Health, The Inga-Britt and Arne Lundberg's Research Foundation, Kidneeds Fund, Olle Engkvist Byggmästare Foundation and The Swedish Freemason's Foundation for Children's Welfare (all to DK). Funding Information: The Swedish Research Council ( 2020-02200, 2017-01920 ), The Knut and Alice Wallenberg Foundation (Wallenberg Clinical Scholar 2015.0320), Skåne Centre of Excellence in Health, The Inga-Britt and Arne Lundberg’s Research Foundation, Kidneeds Fund, Olle Engkvist Byggmästare Foundation and The Swedish Freemason’s Foundation for Children’s Welfare (all to DK).en
dc.description.versionPeer revieweden
dc.format.extent5
dc.format.extent1195769
dc.format.extent1097-1101
dc.identifier.citationAradottir, S S, Kristoffersson, A-C, Jensson, B O, Sulem, P, Gong, H, Pálsson, R & Karpman, D 2023, 'Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome', Kidney International Reports, vol. 8, no. 5, pp. 1097-1101. https://doi.org/10.1016/j.ekir.2023.02.1069en
dc.identifier.doi10.1016/j.ekir.2023.02.1069
dc.identifier.issn2468-0249
dc.identifier.other136726752
dc.identifier.other6eb8254f-03c6-4dfc-8cf5-3bb7b193fb83
dc.identifier.other37180503
dc.identifier.otherPubMedCentral: PMC10166735
dc.identifier.other85149656643
dc.identifier.otherunpaywall: 10.1016/j.ekir.2023.02.1069
dc.identifier.urihttps://hdl.handle.net/20.500.11815/7200
dc.language.isoen
dc.relation.ispartofseriesKidney International Reports; 8(5)en
dc.relation.urlhttps://www.scopus.com/pages/publications/85149656643en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.subjectatypical hemolytic uremic syndromeen
dc.subjectcomplementen
dc.subjectFactor Ben
dc.subjectgeneticsen
dc.subjectmonozygotic twinsen
dc.subjectNephrologyen
dc.titleFactor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndromeen
dc.type/dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/letteren

Skrár

Original bundle

Niðurstöður 1 - 1 af 1
Nafn:
1_s2.0_S246802492301166X_main.pdf
Stærð:
1.14 MB
Snið:
Adobe Portable Document Format
Hlaða niður

Undirflokkur

Háskóli Íslands

Öll gögn í Opnum vísindum eru vernduð af ákvæðum höfundalaga og með öllum réttindum áskildum, nema annað sé tekið fram.