MELAS a clinically and genetically heterogeneous syndrome

Author:

Casique Liliana,De Lucca Marisel,Mahfoud Antonieta,Luis Ramírez José

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference5 articles.

1. Independent origin for M.3243A>G mitochondrial mutation in three venezuelan cases of melas syndrome;Florez;Clin. Biochem.,2022

2. Efficacy and safety of the ketogenic diet for mitochondrial disease with epilepsy: A prospective, open labeled, controlled study;Huang;Front. Neurol.,2022

3. mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease;Grady;EMBO Mol. Med.,2018

4. Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies;Liu;Acta Neurologica Scandinavica,2006

5. Mutation loads in different tissues from six pathogenic mtDNA point mutations;O’Callaghan;Mitochondrion,2015

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