Načítá se...
Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus
Mental retardation (MR) is not a common feature observed in patients with classical ectodermal dysplasias (EDs). Several genes responsible for EDs and MR have been identified. However, the causation has yet to be identified in a significant number of patients with either ED or MR. Here, we have mole...
Uloženo v:
| Hlavní autoři: | , , , , , |
|---|---|
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group
2009
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2605173/ https://ncbi.nlm.nih.gov/pubmed/18854857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.183 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|