Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease

Journal of Molecular Biology

Volumn 277, Issue 3, 1998, Pages 513-517

  Burwinkel, Barbara ^a   Kilimann, Manfred W ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

Glycogen storage disease; L1 element; Phosphorylase kinase; Repetitive genetic element; Retrotransposon

Indexed keywords

DNA; GLYCOGEN; PHOSPHORYLASE KINASE;

ARTICLE; CONTROLLED STUDY; DELETION MUTANT; DNA RECOMBINATION; DNA SEQUENCE; ENZYME SUBUNIT; EXON; GENE MUTATION; GENETIC DISORDER; GLYCOGEN STORAGE DISEASE; HUMAN; PRIORITY JOURNAL;

EID: 0032478502     PISSN: 00222836     EISSN: None     Source Type: Journal    
DOI: 10.1006/jmbi.1998.1641     Document Type: Editorial

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