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Q34507229-E8775436-FA41-41D0-BEEC-15282AE47033
Q34507229-E8775436-FA41-41D0-BEEC-15282AE47033
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34507229-E8775436-FA41-41D0-BEEC-15282AE47033
The NEMO mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation.
P2860
Q34507229-E8775436-FA41-41D0-BEEC-15282AE47033
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34507229-E8775436-FA41-41D0-BEEC-15282AE47033
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Statement
wasDerivedFrom
c977a50e3a1f77e1b13a3c01d1fb17683d1a37e8
P2860
A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)