Načítá se...
Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis
BACKGROUND: Hypohidrotic ectodermal dysplasia (HED) is the most common form of ectodermal dysplasia and is mainly associated with mutations in the EDA, EDAR, and EDARADD responsible for the development of ectodermal‐derived structures. HED displays different modes of inheritance according to the gen...
Uloženo v:
| Vydáno v: | Mol Genet Genomic Med |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2020
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7963410/ https://ncbi.nlm.nih.gov/pubmed/33205897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1555 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|