A Novel Heterozygous Point Mutation in the p63 Gene in a Patient with Ectodermal Dysplasia Associated with B‐Cell Leukemia
Author:
Affiliation:
1. Department of Dermatology, Complejo Hospitalario Arquitecto Marcide‐Novoa Santos, Ferrol, Spain
2. Department of Dermatology, Hospital Niño Jesús, Madrid, Spain
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1525-1470.2011.01474.x
Reference15 articles.
1. p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development
2. p63-Associated Disorders
3. Contribution of p53, p63, and p73 to the developmental diseases and cancer;Tomkova K;Neoplasma,2008
4. Molecular evidence that AEC syndrome and Rapp-Hodgkin syndrome are variable expression of a single genetic disorder
5. Spectrum of Phenotypic Manifestations from a Single Point Mutation of the p63 Gene, Including New Cutaneous and Immunologic Findings
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1. Tooth agenesis and orofacial clefting: genetic brothers in arms?;Human Genetics;2016-10-03
2. p63 steps into the limelight: crucial roles in the suppression of tumorigenesis and metastasis;Nature Reviews Cancer;2013-01-24
3. Role of p53 family members p73 and p63 in human hematological malignancies;Leukemia & Lymphoma;2012-05-21
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