Login
Search
Login
Search
E-Poster Portal
The International Child Neurology Congresses
ePosters
Presenters
Search
Search
You are here:
Home
492.Homozygous mutation in cwf19l1 with recessive ataxia syndrome in a turkish child
Details
Faruk Incecik
Category:
ePosters
Hits: 38
Faruk Incecik
Previous article: 491.Hereditary spastic paraplegia type 26 with a novel mutation in b4galnt1 gene and literature review of the clinical features
Prev
Next article: 493.Gabapentin: efficacy and tolerability as adjuvant therapy for dystonic cerebral palsy
Next