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Paper Details

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.
Cell
547
1999
/EEC interval, EEC, EEC syndrome, EEC-like disorder, LMS, amino acid, autosomal dominant disorder, chromosome 3q27, ectodermal dysplasia, ectrodactyly, facial clefts, homolog of, limb mammary syndrome, mutant p63 isotypes, p53, p63, p63 gene, p63 mutations, p63alpha, p63beta, p63gamma isotypes

Datasets

Release 1.2