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SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9
Known as:
COENZYME Q10 DEFICIENCY, PRIMARY, 4
, Cerebellar Ataxia, Autosomal Recessive, Type 2
, SCAR9
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National Institutes of Health
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Related topics
Related topics
7 relations
ADCK3 gene
Acidosis, Lactic
Autosomal recessive inheritance
Cerebellar Ataxia
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Broader (1)
Ataxia, Spinocerebellar
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Primary Coenzyme Q deficiency Due to Novel ADCK3 Variants, Studies in Fibroblasts and Review of Literature
A. Shalata
,
Michael Edery
,
+11 authors
Ann Saada
Neurochemical Research
2019
Corpus ID: 106409416
Primary deficiency of coenzyme Q10 (CoQ10 ubiquinone), is classified as a mitochondrial respiratory chain disorder with…
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