Case Report FBN1 mutation screening in South African patients with Marfan syndrome

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dc.article.end-page7en
dc.article.start-page1en
dc.citation.doi10.3389/FGENE.2025.1612411en
dc.contributor.authorFelicity Mhlongoen
dc.contributor.authorCandice Febenen
dc.contributor.authorAmanda Krauseen
dc.contributor.authorNadia Carstensen
dc.date.accessioned2025-08-28T11:10:09Z
dc.facultyFACULTY OF HEALTH SCIENCESen
dc.identifier.citationWOSen
dc.identifier.urihttps://hdl.handle.net/10539/46131
dc.journal.titleCase Report FBN1 mutation screening in South African patients with Marfan syndromeen
dc.journal.volume16en
dc.titleCase Report FBN1 mutation screening in South African patients with Marfan syndromeen
dc.typeJournal Articleen

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