Φορτώνει......
Mutational Analysis of Methyl‐CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome
Rett syndrome (RTT) is an X‐linked postnatal neurological disorder, primarily affecting females and characterized by regression, epilepsy, stereotypical hand movements, and motor abnormalities. Its prevalence is about 1 in 10,000 female births. RTT is caused by mutations within methyl CpG‐binding pr...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Clin Lab Anal |
|---|---|
| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
John Wiley and Sons Inc.
2013
|
| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807519/ https://ncbi.nlm.nih.gov/pubmed/23400946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21574 |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|