Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-γ)

American Journal of Human Genetics

Volumn 68, Issue 3, 2001, Pages 765-771

  Aradhya, Swaroop ^a   Courtois, Gilles ^b   Rajkovic, Aleks ^a   Lewis, Richard Alan ^a   Levy, Moise ^a   Israël, Alain ^b   Nelson, David L ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b INSTITUT PASTEUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSINE; ZINC FINGER PROTEIN;

APOPTOSIS; ARTICLE; CARBOXY TERMINAL SEQUENCE; CLINICAL ARTICLE; FEMALE; GENE DELETION; GENE DUPLICATION; GENE MUTATION; HUMAN; INCONTINENTIA PIGMENTI; LETHALITY; MALE; PHENOTYPE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; X CHROMOSOME DOMINANT INHERITANCE; X CHROMOSOME INACTIVATION;

EID: 0035089759     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318806     Document Type: Article

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