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Succinate-Coa Ligase Deficiency

Known as: Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, with Mild Methylmalonic Aciduria, Mitochondrial Dna Depletion, Encephalomyopathic Form, with Methylmalonic Aciduria, Succinate-Coenzyme A Ligase Deficiency 
 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Mitochondrial Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
A new pathogenic homozygous variant in deoxyguanosine kinase gene cause vital progressive liver failure in a neonate: case report
Background: Mitochondrial DNA-depletion syndromes (MDDS) usually present with a wide spectrum of clinical manifestations, such as… Expand
Review
2014
Review
2014
[SUCLA2-related encephalomyopathic mitochondrial DNA depletion syndrome: a case report and review of literature].
OBJECTIVE To analyze the clinical characteristics of SUCLA2-related encephalomyopathic mitochondrial DNA depletion syndrome (MDS… Expand
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