| Autor: |
Iglesias, Diana, Palmitano, Juan, Arrizurieta, Elvira, Kornblihtt, Alberto, Herrera, Mariana, Bernath, Viviana, Martin, Rodolfo, Iglesias, D M, Palmitano, J A, Arrizurieta, E, Kornblihtt, A R, Herrera, M, Bernath, V, Martin, R S |
| Zdroj: |
Digestive Diseases & Sciences; Feb1999, Vol. 44 Issue 2, p385-388, 4p |
| Abstrakt: |
Autosomal dominant polycystic liver disease occurs commonly in association with autosomal dominant polycystic kidney disease, types 1 and 2. It may also exist as a separate entity, genetically distinct from autosomal dominant polycystic kidney disease types 1 and 2, as has been recently established to exist in a Belgian family. We report here a large Argentinian family of Spanish-Belgian ancestry with autosomal dominant polycystic liver disease, where proximal and distal markers for both polycystic kidney disease 1 and 2 failed to demonstrate genetic linkage. The data support the notion that polycystic liver disease and autosomal dominant polycystic kidney disease may have separate chromosomal loci. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
Full text from SpringerLink