Female Patient Showing Hypohidrotic Ectodermal Dysplasia and Immunodeficiency (HED-ID)
- 1 September 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 69 (3) , 664-665
- https://doi.org/10.1086/323003
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmentiNature, 2000
- Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti type 2Human Molecular Genetics, 1996
- Familial linear and whorled nevoid hypermelanosisJournal of the American Academy of Dermatology, 1994