HLA COMPLEX IN WERNER'S DISEASE

dc.creatorPerez-Rojas, G.
dc.creatorMarcano, N.
dc.creatorGonzalez, L.
dc.creatorPenchaszadeh, G.
dc.creatorMoya, P.
dc.creatorBianco Colmenares, Nicolás E.
dc.creatorAbadí, Isaac.
dc.date2016-12-07T17:22:32Z
dc.date2016-12-07T17:22:32Z
dc.date1979-11-23
dc.date.accessioned2022-10-28T01:19:45Z
dc.date.available2022-10-28T01:19:45Z
dc.identifierhttp://hdl.handle.net/10872/13906
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4947550
dc.descriptionDuring the 8th International Workshop, we studied family 01, where five patients with Werner's disease were identified in the first generation. Werner's Syndrome is a rare entity with a recessive pattern of inheritance where consanguinity between parents is expected to be increased . In our family we found that individuals 300 and 301 were first cousins It is relevant at this point to rep ort that this family comes from Quibor, a small town in Venezuela, where a group of German immigrants sett led in the middle of t he 19th century, creating a highly inbred population. Quibor still maintains some German characteristics in architecture, habits, and people with Caucasian features.
dc.languageen
dc.publisherClinical Immunology National Center and National Center for Rheumatic Diseases, SAS-UCV.
dc.subjectWerner's Syndrome
dc.subjectrecessive pattern
dc.subjectinheritance
dc.subjectconsanguinity
dc.subjectfamily
dc.subjectindividuals
dc.titleHLA COMPLEX IN WERNER'S DISEASE
dc.typeArticle


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