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Results: 1 to 7 of 7
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Mitochondrial Genome Sequencing and Depletion/Integrity Panel Molecular Genetics Laboratory London Health Sciences Centre Canada | 47 | 52 |
|
Neuropathy, Ataxia and Retinis pigmentosa (NARP) : T8993G mutation study Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 1 | 1 |
|
Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 4 | 3 |
|
Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 9 | 17 |
|
65 mtDNA Point Mutations plus Large Deletions Panel GeneDx United States | 17 | 65 |
|
Common Mitochondrial Disorders Evaluation (POLG, MELAS, MERRF, NARP) Athena Diagnostics Inc United States | 6 | 4 |
|
NARP syndrome (neuropathy, ataxia and retinitis pigmentosa): Mutation analysis (T8993G) GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 1 | 1 |
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Results: 1 to 7 of 7
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