Identification of coding variants associated with familial systemic lupus erythematosus through whole exome sequencing

dc.contributor.advisorTiffin, Nicki
dc.contributor.authorvan Vuuren, Larry Peter
dc.date.accessioned2018-07-30T10:13:09Z
dc.date.accessioned2024-05-17T07:57:56Z
dc.date.available2018-08-31T22:10:06Z
dc.date.available2024-05-17T07:57:56Z
dc.date.issued2016
dc.descriptionPhilosophiae Doctor - PhD (Bioinformatics)
dc.description.abstractSystemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease characterized by the production of a wide range of autoantibodies directed against selfantigens. SLE can influence almost any organ system and its appearance and course are highly varied, ranging from remission to disease flare. SLE demonstrates a variety of constitutional symptoms, such as the skin, musculoskeletal and mild hematologic involvement. On the other hand, some patients present with primarily hematologic, renal or neuropsychiatric manifestations.
dc.identifier.urihttps://hdl.handle.net/10566/15284
dc.language.isoen
dc.publisherUniversity of the Western Cape
dc.rights.holderUniversity of the Western Cape
dc.titleIdentification of coding variants associated with familial systemic lupus erythematosus through whole exome sequencing

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