CHCHD10
CHCHD10, whose full official name is coiled-coil-helix-coiled-coil-helix domain containing 10, is a gene found in Humans encoding a mitochondrial protein that is enriched at cristae junctions in the intermembrane space. It may play a role in cristae morphology maintenance or oxidative phosphorylation. CHCHD10-related disorders include mitochondrial myopathy,[1] amyotrophic lateral sclerosis (ALS),[2] frontotemporal dementia (FTD),[2] late-onset spinal motor neuronopathy (SMAJ), and cerebellar ataxia. Alternative splicing of this gene results in multiple transcript variants.
References
This article incorporates text from the United States National Library of Medicine ([1]), which is in the public domain.
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