Atypical Forms of Incontinentia Pigmenti in Male Individuals Result from Mutations of a Cytosine Tract in Exon 10 of NEMO (IKK-γ)
- 1 March 2001
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 68 (3), 765-771
- https://doi.org/10.1086/318806
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
- The Ectodermal Dysplasia Receptor Activates the Nuclear Factor-κB, JNK, and Cell Death Pathways and Binds to Ectodysplasin APublished by Elsevier BV ,2001
- NEMO/IKKγ-Deficient Mice Model Incontinentia PigmentiMolecular Cell, 2000
- Control of apoptosis by Rel/NF-κB transcription factorsOncogene, 1999
- X‐inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationClinical Genetics, 1999
- Male cases of incontinentia pigmenti: Case report and reviewAmerican Journal of Medical Genetics, 1998
- Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti type 2Human Molecular Genetics, 1996
- Gonadal mosaicism for incontinentia pigmenti in a healthy male.Journal of Medical Genetics, 1995
- Immunologic Investigations in Eight Patients with Incontinentia PigmentiPediatric Dermatology, 1990
- Incontinentia pigmenti: A failure of immune tolerance?Journal of the American Academy of Dermatology, 1985
- Incontinentia pigmenti. Evidence for both neutrophil and lymphocyte dysfunctionArchives of Dermatology, 1978