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Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2
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229 Cysteine and homocysteine can be interconverted through the sulfur transfer pathway
They also include single, large-scale mtDNA deletions which can either be inherited or arise sporadically during embryogenesis [2]
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*Correspondence: Jana Frahm, [email protected] Disclaimer All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers
