Φορτώνει......
The clinical features and diagnosis of Metachromatic leukodystrophy: A case series of Iranian Pediatric Patients
OBJECTIVE: Metachromatic leukodystrophy disorder (MLD) is one of the rare neurometabolic diseases caused due to lack of saposin B and arylsulfatase A enzyme deficiency. MATERIALS & METHODS: Eighteen patients diagnosed as metachromatic leukodystrophy in the Neurology Department of Mofid Children’...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Iran J Child Neurol |
|---|---|
| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Shahid Beheshti University of Medical Sciences
2015
|
| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4577699/ https://ncbi.nlm.nih.gov/pubmed/26401154 |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|