Chargement en cours...
Rett Syndrome in Males: The Different Clinical Course in Two Brothers with the Same Microduplication MECP2 Xq28
Rett syndrome (RTT) is a neurodevelopmental disorder with a genetic basis that is associated with the mutation of the X-linked methyl-CpG binding protein 2 (MECP2) gene in approximately 90% of patients. RTT is characterized by a brief period of normal development followed by loss of acquired skills...
Enregistré dans:
| Publié dans: | Int J Environ Res Public Health |
|---|---|
| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
MDPI
2019
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6747413/ https://ncbi.nlm.nih.gov/pubmed/31450876 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijerph16173075 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|