Srp Arh Celok Lek
 2015
DOI: 10.2298/sarh1512752m
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A novel frameshift mutation of the IKBKG gene causing typical incontinentia pigmenti

Snežana Minić
1
,
Dušan Trpinac2,
Miljana Obradović3

Abstract: The registered novel frameshift/KBKG mutation c.641_647delGCATGGAinsAT (p.Arg214HisfsX38) can be considered to be the cause of IP in this case.

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