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

Epidermal growth factor receptor (EGFR), a receptor that recognizes epidermal growth factor, is a very important regulator of cell proliferation and differentiation. To date, three cases of severe ectodermal dysplasia were reported to be caused by an inherited germline homozygous loss-of-function mi...

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Detalles Bibliográficos
Autores principales: Hayashi, Shion, Yokoi, Takayuki, Hatano, Chihiro, Enomoto, Yumi, Tsurusaki, Yoshinori, Naruto, Takuya, Kobayashi, Masahisa, Ida, Hiroyuki, Kurosawa, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993725/
https://www.ncbi.nlm.nih.gov/pubmed/29899996
http://dx.doi.org/10.1038/s41439-018-0011-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993725/
https://www.ncbi.nlm.nih.gov/pubmed/29899996
http://dx.doi.org/10.1038/s41439-018-0011-0

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