euL1db
The European database of L1-HS retrotransposon insertions in humans

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Study ID   Van_den_Hurk2003
Citation:  
van den Hurk, J.A., van de Pol, D.J., Wissinger, B., van Driel, M.A., Hoefsloot, L.H., de Wijs, I.J., van den Born, L.I., Heckenlively, J.R., Brunner, H.G., et al. (2003) Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exon. Hum Genet, 113, 268-275.
Pubmed:   PMID:12827496




         Description
Novel types of mutation in the choroideremia ( CHM) gene: a full-length L1insertion and an intronic mutation activating a cryptic exon.


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