Vedrana M. Rasic
Belgrade, SE, Serbia
Last Updated: 09/26/2026
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Found 10 publications
Biallelic variants in COX18 cause a mitochondrial disorder primarily manifesting as peripheral neuropathy.
Journal: medRxiv : the preprint server for health sciences
Published: July 15, 2024
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database.
Journal: Journal of neuromuscular diseases
Published: November 11, 2017
GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia.
Journal: Parkinsonism & related disorders
Published: April 17, 2017
A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian population.
Journal: European journal of human genetics : EJHG
Published: July 26, 2016
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
Journal: Human mutation
Published: November 18, 2014
Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2.
Journal: American journal of human genetics
Published: July 31, 2014
ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency.
Journal: Journal of neurology
Published: June 11, 2014
Mapping the differences in care for 5,000 spinal muscular atrophy patients, a survey of 24 national registries in North America, Australasia and Europe.
Journal: Journal of neurology
Published: August 20, 2013
Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.
Journal: Nature genetics
Published: February 23, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026