Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference49 articles.
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3. EEC-LM-ADULT syndrome caused by R319H mutation in TP63 with ectrodactyly, syndactyly, and teeth anomaly;Medicine;2020-10-30
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