Condition: RAPP-HODGKIN SYNDROME
rs121908840 in
TP63 gene and
RAPP-HODGKIN SYNDROME
PMID 12939657 2003 The Rapp-Hodgkin syndrome results from mutations of the TP63 gene.
PMID 15200513 2004 Molecular evidence that AEC syndrome and Rapp-Hodgkin syndrome are variable expression of a single genetic disorder.
PMID 12766194 2003 Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia.