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http://hdl.handle.net/10872/13906
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| Título : | HLA COMPLEX IN WERNER'S DISEASE |
| Autor : | Perez-Rojas, G.
Marcano, N.
Gonzalez, L.
Penchaszadeh, G.
Moya, P.
Bianco Colmenares, Nicolás E.
Abadí, Isaac. |
| Palabras clave : | Werner's Syndrome
recessive pattern
inheritance
consanguinity
family
individuals |
| Fecha de publicación : | 23-Nov-1979 |
| Editorial : | Clinical Immunology National Center and National Center for Rheumatic Diseases, SAS-UCV. |
| Resumen : | During 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. |
| URI : | http://hdl.handle.net/10872/13906 |
| Aparece en las colecciones: | Artículos Publicados
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