Title : Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency.

Pub. Date : 2014 Jan

PMID : 24498631






3 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Mutations in Fe-S proteins often disrupt Fe-S cluster assembly leading to a spectrum of severe disorders such as Friedreich"s ataxia or iron-sulfur cluster assembly enzyme (ISCU) myopathy. Iron iron-sulfur cluster assembly enzyme Homo sapiens
2 Mutations in Fe-S proteins often disrupt Fe-S cluster assembly leading to a spectrum of severe disorders such as Friedreich"s ataxia or iron-sulfur cluster assembly enzyme (ISCU) myopathy. Iron iron-sulfur cluster assembly enzyme Homo sapiens
3 Mutations in Fe-S proteins often disrupt Fe-S cluster assembly leading to a spectrum of severe disorders such as Friedreich"s ataxia or iron-sulfur cluster assembly enzyme (ISCU) myopathy. Iron iron-sulfur cluster assembly enzyme Homo sapiens