Associated Papers
WNT10B mutations associated with isolated dental anomalies.
Kantaputra PN et al.
Clinical Genetics, 2018
Insight into IKBKG/NEMO locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease.
Conte MI et al.
Human Mutation, 2014
Incontinentia pigmenti revisited. A novel nonsense mutation of the IKBKG gene.
Fryssira H et al.
Acta Paediatrica (oslo, Norway : 1992), 2011
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