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C19orf12 gene

Known as: CHROMOSOME 19 OPEN READING FRAME 12, C19ORF12, NBIA4 
National Institutes of Health

Related topics

Related topics

1 relation
Neuroferritinopathy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Mutation screening of SLC52A3, C19orf12, and TARDBP in Iranian ALS patients
2017
2017
The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN.
2017
2017
Mutations in C19orf12 and intronic repeat expansions in C9orf72 not observed in Iranian Parkinson's disease patients
2016
2016
Mitochondrial Membrane Protein-Associated Neurodegeneration Mimicking Juvenile Amyotrophic Lateral Sclerosis.
Review
2015
Review
2015
Mitochondria: A crossroads for lipid metabolism defect in neurodegeneration with brain iron accumulation diseases.
2015
2015
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation.
2014
2014
Mitochondrial protein associated neurodegeneration - case report.
2014
2014
[A new form of hereditary neurodegeneration with brain iron accumulation: clinical and molecular-genetic characteristics].
Neurodegeneration with brain iron accumulation, type 4 (NBIA4, or MPAN) is an autosomal recessive disease produced by С19org12… 
2013
2013
PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation
Neurodegeneration with brain iron accumulation (NBIA) constitutes a group of neurodegenerative disorders with pronounced iron… 
2013
2013
Rapid disease progression in adult‐onset mitochondrial membrane protein‐associated neurodegeneration
Neurodegeneration with brain iron accumulation (NBIA) comprises a clinically and genetically heterogeneous group of… 
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