p63-Associated Disorders

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p63-associated disorders.

Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics. Different combinations of these features are seen in five different syndromes, of which ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome (EEC) is the most common one. Mutations in p63 can...

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A step closer toward therapies for p63-related disorders

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ژورنال

عنوان ژورنال: Cell Cycle

سال: 2007

ISSN: 1538-4101,1551-4005

DOI: 10.4161/cc.6.3.3796