A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies
Sareh Hosseinpour(Imam Khomeini Hospital), Ali Reza Tavasoli(Children's Medical Center), Masoud Garshasbi(Max Planck Institute for Molecular Genetics), Homa Ghabeli(Children's Medical Center), Mahmoud Reza Ashrafi(Children's Medical Center), Zahra Zamani(Tehran University of Medical Sciences), Maryam Rasulinezhad(Iran University of Medical Sciences), Ali Ahani(Iran University of Medical Sciences), Reyhaneh Kameli(Children's Medical Center), Mohammad Ghafouri(Temple University), Nejat Mahdieh(Iran University of Medical Sciences), Ali Zare Dehnavi(Children's Medical Center), Morteza Heidari(Tehran University of Medical Sciences), Reza Shervin Badv(Children's Medical Center), Hassan Vahidnezhad(Children's Hospital of Philadelphia), Sasan Saket(Shahid Beheshti University of Medical Sciences), Ehsan Razmara(Tarbiat Modares University), Reza Azizi Malamiri(Ahvaz Jundishapur University of Medical Sciences), Neda Pak(Children's Medical Center), Ali Hosseini Bereshneh(Shiraz University of Medical Sciences), Bahram Mohammadi(Children's Medical Center), Zahra Rezaei(Iran University of Medical Sciences), Mahmoud Mohammadi(Children's Medical Center), Gholam Reza Zamani(Tehran University of Medical Sciences), Bahareh Rabbani(Tehran University of Medical Sciences)
Cited by 2
Related Papers
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
|The American Journal of Human Genetics|2012|273
HIV-1 associated dementia: symptoms and causes
|Retrovirology|2006|214
Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene
|The American Journal of Human Genetics|2010|208
Efficacy and safety of intravenous sodium valproate versus phenobarbital in controlling convulsive status epilepticus and acute prolonged convulsive seizures in children: A randomised trial
|European Journal of Paediatric Neurology|2012|91