mtSEEK® Mitochondrial Genome Sequencing method(s): ◦ Sequencing, Next Gen Courtagen Life Sciences, Courtagen Diagnostics Laboratory - Woburn, MA, USA |
Mitochondrial Disorders (mtDNA) Sequencing method(s): ◦ Sequencing, Next Gen ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA |
Mitochondrial Disorders Panel (mtDNA Sequencing and Deletion/Duplication, 121 Nuclear Genes Sequencing, 119 Nuclear Genes Deletion/Duplication) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA |
Leber Hereditary Optic Neuropathy method(s): ◦ Sequencing, Capillary (Sanger) L.E.S. Mikrogen Genetic Diagnosis Center - Ankara, Turkey |
Mitochondrial Disorders method(s): ◦ Sequencing, Capillary (Sanger) L.E.S. Mikrogen Genetic Diagnosis Center - Ankara, Turkey |
Leigh Syndrome (nuclear DNA mutation) Test method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Mitochondrial Disorders Test method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
mtDNA encoded Mitochondriopathies Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
Mitochondrial Disorders, Panel Massive Sequencing 37 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Leber optic atrophy (sequence analysis of MTND4L gene) method(s): ◦ Sequencing, Capillary (Sanger) CGC Genetics - Porto, Portugal |
Mitochondrial complex I deficiency method(s): ◦ Sequencing, Capillary (Sanger) Centogene AG, Rare Disease Company - Rostock, Germany |
Leber optic atrophy method(s): ◦ Sequencing, Capillary (Sanger) Centogene AG, Rare Disease Company - Rostock, Germany |
Mitochondrial Genome NGS Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Fulgent Diagnostics - Temple City, CA, USA |
CentoMito™ Genome method(s): ◦ Sequencing, Next Gen Centogene AG, Rare Disease Company - Rostock, Germany |
Leber optic atrophy panel method(s): ◦ Sequencing, Next Gen Centogene AG, Rare Disease Company - Rostock, Germany |