Sir, In 2014, we provided a genetic basis to support the conclusion that mitochondrial
dysfunction can have a causative effect in motor neuron degeneration. We reported a large …

We read with interest the recent publication in Brain by Bannwarth et al.(2014a) identifying
CHCHD10 mutations in patients with frontotemporal dementia-amyotrophic lateral sclerosis …

Many genes have been found to be pathogenic for amyotrophic lateral sclerosis (ALS).
Among them, the coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10) has …

Sir, Recently, a study identified a mutation (c. 176C> T, p. S59L) in the CHCHD10 gene as a
cause of amyotrophic lateral sclerosis (ALS)/frontotemporal dementia (FTD) in a large …

CHCHD10 gene has been identified to be associated with frontotemporal dementia (FTD)
and amyotrophic lateral sclerosis (ALS). Considering the clinical phenotype and pathology …

Sir, We read with interest the paper recently published in Brain (Bannwarth et al., 2014)
reporting a mutation in CHCHD10 (c. 176C> T, p. Ser59Leu) in familial amyotrophic lateral …

Mutations in the CHCHD10 gene have been recently identified in a large family with a
complex phenotype variably associating frontotemporal dementia (FTD) with amyotrophic …

Sir, A recent study by Bannwarth and colleagues has shown that variation in the CHCHD10
gene is a cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia …

Sir, Emerging data provide evidence for CHCHD10 as a new candidate gene in familial
amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD)(Bannwarth et al …

Coiled-coil-helix-coiled-coil-helix domain containing 2 (CHCHD2) and Coiled-coil-helix-
coiled-coil-helix domain containing 10 (CHCHD10) are mitochondrial proteins that are …