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Human Molecular Genetics|August 6, 2008

A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in functionMarco Spinazzi, Silvia Cazzola, Mario Bortolozzi, et al.

Scientific Reports|January 25, 2017

Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubesCarmelo Milioto, Adriana Malena, Eleonora Maino, et al.

American Journal of Human Genetics|June 4, 2016

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain DeficiencyRikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, et al.

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Showing results (11-20 of 13) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 13 results.

Human Molecular Genetics|August 6, 2008

A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in functionMarco Spinazzi, Silvia Cazzola, Mario Bortolozzi, et al.

Scientific Reports|January 25, 2017

Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubesCarmelo Milioto, Adriana Malena, Eleonora Maino, et al.

American Journal of Human Genetics|June 4, 2016

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain DeficiencyRikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, et al.

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