LINE-1 Elements at the Sites of Molecular Rearrangements in Alport Syndrome–Diffuse Leiomyomatosis
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference28 articles.
1. Hereditary familial congenital haemorrhagic nephritis;Alport;Br Med J,1927
2. Current protocols in molecular biology,1994
3. Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease;Burwinkel;J Mol Biol,1998
4. Diffuse leiomyomatosis in Alport syndrome;Cochat;J Pediatr,1988
5. Current protocols in human genetics,1997
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