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SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9

Known as: COENZYME Q10 DEFICIENCY, PRIMARY, 4, Cerebellar Ataxia, Autosomal Recessive, Type 2, SCAR9 
 
National Institutes of Health

Related topics

Related topics

7 relations
ADCK3 geneAcidosis, LacticAutosomal recessive inheritanceCerebellar Ataxia
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Broader (1)

Ataxia, Spinocerebellar

Papers overview

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Review
2019
Review
2019
Primary Coenzyme Q deficiency Due to Novel ADCK3 Variants, Studies in Fibroblasts and Review of Literature
Primary deficiency of coenzyme Q10 (CoQ10 ubiquinone), is classified as a mitochondrial respiratory chain disorder with… Expand
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