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Life (Basel, Switzerland)|February 25, 2023

Novel ELAC2 Mutations in Individuals Presenting with Variably Severe Neurological Disease in the Presence or Absence of CardiomyopathyCérane Cafournet, Sofia Zanin, Anne Guimier, et al.

Cell Reports|March 4, 2015

The mitochondrial calcium uniporter controls skeletal muscle trophism in vivoCristina Mammucari, Gaia Gherardi, Ilaria Zamparo, et al.

Human Molecular Genetics|July 13, 2016

Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signallingElisa Gregianin, Giorgia Pallafacchina, Sofia Zanin, et al.

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Showing results (21-30 of 23) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 23 results.

Life (Basel, Switzerland)|February 25, 2023

Novel ELAC2 Mutations in Individuals Presenting with Variably Severe Neurological Disease in the Presence or Absence of CardiomyopathyCérane Cafournet, Sofia Zanin, Anne Guimier, et al.

Cell Reports|March 4, 2015

The mitochondrial calcium uniporter controls skeletal muscle trophism in vivoCristina Mammucari, Gaia Gherardi, Ilaria Zamparo, et al.

Human Molecular Genetics|July 13, 2016

Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signallingElisa Gregianin, Giorgia Pallafacchina, Sofia Zanin, et al.

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