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

Home Background Search Browse Utilities Help FAQ Data Contact


Study Page

Study ID   Meischl2000
Citation:  
Meischl, C., Boer, M., Ahlin, A. and Roos, D. (2000) A new exon created by intronic insertion of a rearranged LINE-1 element as the cause of chronic granulomatous disease. Eur J Hum Genet, 8, 697-703.
Pubmed:   PMID:10980575





         Description
A new exon created by intronic insertion of a rearranged LINE-1 element as thecause of chronic granulomatous disease.


Mapped assembly Original assembly Browse by SRIP Browse by MRIP
hg19_NCBI37 . SRIP MRIP