Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - Elsevier
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral
Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p. Gly66Val) in the same gene …

[引用][C] Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - NEUROBIOLOGY …, 2018 - researchportal.tuni.fi
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial
localisation, are likely associated with severity of CHCHD10-related diseases — Tampere …

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - pure.johnshopkins.edu
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral
Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p. Gly66Val) in the same gene …

[HTML][HTML] Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10 …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - ncbi.nlm.nih.gov
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral
Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p. Gly66Val) in the same gene …

[引用][C] Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

E Génin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - hal.science
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial
localisation, are likely associated with severity of CHCHD10-related diseases - Archive …

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - europepmc.org
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral
Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p. Gly66Val) in the same gene …

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - docusalut.com
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral
Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p. Gly66Val) in the same gene …

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of Disease … - dspace.uib.es
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral
Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p. Gly66Val) in the same gene …

[引用][C] Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - cir.nii.ac.jp
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial
localisation, are likely associated with severity of CHCHD10-related diseases | CiNii Research …

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related …

EC Genin, S Bannwarth, F Lespinasse… - Neurobiology of …, 2018 - pubmed.ncbi.nlm.nih.gov
Following the involvement of CHCHD10 in FrontoTemporal-Dementia-Amyotrophic Lateral
Sclerosis (FTD-ALS) clinical spectrum, a founder mutation (p. Gly66Val) in the same gene …