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Search: authors:"Hayley Woffendin"

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A recurrent deletion in the ubiquitously expressed NEMO (IKK-γ) gene accounts for the vast majority of incontinentia pigmenti mutations

, Hayley Woffendin, Tiziana Bardaro and Asmae Smahi should be regarded as joint First Authors deletion alters sequence after nucleotide 399 (from ATG) in the NEMO mRNA and leads to a truncated protein