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

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Study ID   Bernard2009
Citation:  
Bernard, V., Minnerop, M., Bürk, K., Kreuz, F., Gillessen-Kaesbach, G. and Zuhlke, C. (2009) Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2. BMC Med Genet, 10, 87.
Pubmed:   PMID:19744353





         Description
Exon deletions and intragenic insertions are not rare in ataxia with oculomotor apraxia 2.


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