A novel SVA retrotransposon insertion in the CHM gene results in loss of REP-1 causing choroideremia

Single-base substitutions in the CHM promoter as a cause of choroideremia

(2017) Alina Radziwon et al.   HUMAN MUTATION

Roles for retrotransposon insertions in human disease

(2016) Dustin C. Hancks et al.   Mobile DNA

Copy Number Variant Analysis in CHM to Detect Duplications Underlying Choroideremia

(2012) Jonathan Y. Chi et al.   OPHTHALMIC GENETICS

Retrotransposition of marked SVA elements by human L1s in cultured cells

(2011) Dustin C. Hancks et al.   HUMAN MOLECULAR GENETICS

Exon-trapping mediated by the human retrotransposon SVA

(2009) D. C. Hancks et al.   GENOME RESEARCH

5'-Transducing SVA retrotransposon groups spread efficiently throughout the human genome

(2009) A. Damert et al.   GENOME RESEARCH

An alternative pathway for Alu retrotransposition suggests a role in DNA double-strand break repair

(2008) Deepa Srikanta et al.   GENOMICS