Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease 1 1Edited by J. Karn
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Structural Biology
Reference34 articles.
1. LINEs and Alus – the polyA connection;Boeke;Nature Genet.,1997
2. Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase β subunit (PHKB);Burwinkel;Hum. Mol. Genet.,1997
3. Human Gene Mutation;Cooper,1993
4. Molecular characterization of a novel 10.3 kb deletion causing β-thalassaemia with unusually high Hb A2;Craig;Brit. J. Haematol.,1992
5. A LINE element is present at the site of a 300-kb deletion starting in intron 10 of the PAX6 gene in a case of familial aniridia;Drechsler;Hum. Genet.,1996
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