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Hypohidrotic Ectodermal Dysplasia and Immunodeficiency with Coincident NEMO and EDA Mutations
Ectodermal dysplasias (ED) are uncommon genetic disorders resulting in abnormalities in ectodermally derived structures. Many ED-associated genes have been described, of which ectodysplasin-A (EDA) is one of the more common. The NF-κB essential modulator (NEMO encoded by the IKBKG gene) is unique in...
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Main Authors: | , , , , , , , , , , , |
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格式: | Artigo |
語言: | Inglês |
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Frontiers Research Foundation
2011
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主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3341983/ https://ncbi.nlm.nih.gov/pubmed/22566850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2011.00061 |
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