A new mutation in TP63 is associated with age-related pathology

European Journal of Human Genetics

Volumn 15, Issue 11, 2007, Pages 1115-1120

  Holder Espinasse, Muriel ^a   Martin Coignard, Dominique ^b   Escande, Fabienne ^a   Manouvrier Hanu, Sylvie ^a  

^a LILLE UNIVERSITY HOSPITAL   (France)

^b Centre Hospitalier du Mans   (France)

Author keywords

Corneal dystrophy; Premature menopause; Rapp odgkin syndrome; TP63

Indexed keywords

PROTEIN P53; PROTEIN TP63; UNCLASSIFIED DRUG;

ADULT; AGE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHROMOSOME 3Q; CLEFT LIP PALATE; CLINICAL FEATURE; CORNEA DYSTROPHY; EARLY MENOPAUSE; ECTODERMAL DYSPLASIA; ECTRODACTYLY; FAMILY; FEMALE; GENE MUTATION; HUMAN; PRIORITY JOURNAL; RAPP HODGKIN SYNDROME;

MUS;

EID: 35548991922     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201888     Document Type: Article

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