Genomic architecture at the Incontinentia Pigmenti locus favours de novo pathological alleles through different mechanisms

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Human Molecular Genetics, Vol. 21, Iss. 6, 2012-03 ,pp. : 1260-1271

Oxford University Press

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Identification of a new NEMO/TRAF6 interface affected in incontinentia pigmenti pathology

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Human Molecular Genetics, Vol. 19, Iss. 16, 2010-08 ,pp. : 3138-3149

Oxford University Press

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Somatic mosaicism of a novel IKBKG mutation in a male patient with incontinentia pigmenti

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 7, 2015-07 ,pp. : 1601-1604

John Wiley & Sons Inc

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Skin lesion development in a mouse model of incontinentia pigmenti is triggered by NEMO deficiency in epidermal keratinocytes and requires TNF signaling

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Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 531-542

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The NF-B signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes

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