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- NP797403.RAjF5OUJ05YxWQmMb66ibih1XqZa-lJktZJNjXng66J8o130_assertion type Assertion NP797403.RAjF5OUJ05YxWQmMb66ibih1XqZa-lJktZJNjXng66J8o130_head.
- NP797403.RAjF5OUJ05YxWQmMb66ibih1XqZa-lJktZJNjXng66J8o130_assertion description "[We report the molecular characterization of a new missense mutation of NEMO (A323P) which causes a severe form of incontinentia pigmenti (OMIM#308300), an inherited disease characterized predominantly by skin inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797403.RAjF5OUJ05YxWQmMb66ibih1XqZa-lJktZJNjXng66J8o130_provenance.
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