Epidermal growth factor receptor deficiency: Expanding the phenotype beyond infancy-Reference-Cited by-同舟云学术

Epidermal growth factor receptor deficiency: Expanding the phenotype beyond infancy

Published:2020-06-30 Issue:8 Volume:47 Page:898-902
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Earl Brian R.¹,Szybowska Marta²,Marwaha Ashish³,Belostotsky Vladimir⁴,Lara‐Corrales Irene⁵,Pope Elena⁵,Kannu Peter³^ORCID

Affiliation:

1. Faculty of Medicine University of Toronto Toronto Ontario Canada

2. Fred A. Litwin Family Centre in Genetic Medicine University Health Network Toronto Ontario Canada

3. Division of Clinical and Metabolic Genetics Department of Paediatrics University of Toronto and The Hospital for Sick Children Toronto Ontario Canada

4. Division of Nephrology Department of Paediatrics McMaster University Hamilton Ontario Canada

5. Section of Dermatology Division of Paediatric Medicine University of Toronto and The Hospital for Sick Children Toronto Ontario Canada

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.15377

Reference14 articles.

1. Expression and Function of the Epidermal Growth Factor Receptor in Physiology and Disease

2. The erbB Family: Targets for Therapeutic Development Against Cancer and Therapeutic Strategies Using Monoclonal Antibodies and Tyrosine Kinase Inhibitors

3. Epithelial Inflammation Resulting from an Inherited Loss-of-Function Mutation in EGFR

4. EGFR mutations cause a lethal syndrome of epithelial dysfunction with progeroid features

5. Biallelic mutations of EGFR in a compound heterozygous state cause ectodermal dysplasia with severe skin defects and gastrointestinal dysfunction

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