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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...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2009
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| Assuntos: | |
| Acesso em linha: | 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 |
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