Ectodermal dysplasias: The p63 tail

Giornale Italiano di Dermatologia e Venereologia

Volumn 148, Issue 1, 2013, Pages 53-58

  Tadini, G ^a   Santagada, F ^b   Brena, M ^b   Pezzani, L ^b   Nannini, P ^c  

^a FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c UNIVERSITY OF MILAN   (Italy)

Author keywords

Associated syndromes; Ectodermal dysplasia; Genotype phenotype; p63 mutation

Indexed keywords

ARGININE; ASPARAGINE; GLUTAMINE; PROTEIN P63;

ADULT SYNDROME; AEC SYNDROME; AMINO ACID SUBSTITUTION; CLEFT LIP PALATE; CLEFT PALATE; CLINODACTYLY; DNA BINDING; DRY SKIN; ECTODERMAL DYSPLASIA; ECTRODACTYLY; EEC SYNDROME; GAIN OF FUNCTION MUTATION; GENE DELETION; GENE EXPRESSION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPODONTIA; LMS SYNDROME; MISSENSE MUTATION; NAIL DYSTROPHY; NIPPLE MALFORMATION; ONTOGENY; PHENOTYPE; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN STABILITY; REVIEW; RHS SYNDROME; SCANTY HAIR; SHFM SYNDROME; SYNDACTYLY;

EID: 84876538156     PISSN: 03920488     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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