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Results: 1 to 14 of 14 (representing 12 labs)

Tests names and labsConditionsGenes and analytesMethods

Mitochondrial Genome Sequence

Molecular Genetics Laboratory London Health Sciences Centre
Canada
2238
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MT-ATP6. Detection of the mutations m.8993T>G and m.8993T>C by sequencing

Instituto de Medicina Genomica
Spain
11
  • E Sequence analysis of select exons

MTATP6. Detection of the mutations m.8993T>G and m.8993T>C by sequencing

Instituto de Medicina Genomica
Spain
11
  • T Targeted variant analysis

Neuropathy, Ataxia and Retinis pigmentosa (NARP) : T8993G mutation study

Foundation for Research In Genetics and Endocrinology and Institute of Human Genetics Institute of Human Genetics
India
11
  • T Targeted variant analysis

Myoclonic epilepsy with ragged-red fibers(MERRF), Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes(MELAS), LEIGH, Neuropathy,Ataxia and retinis pigmentosa(NARP) mutations study

Foundation for Research In Genetics and Endocrinology and Institute of Human Genetics Institute of Human Genetics
India
43
  • T Targeted variant analysis

NARP syndrome

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Common Mitochondrial Disorders Evaluation (POLG, MELAS, MERRF, NARP)

Athena Diagnostics Inc
United States
64
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

NARP syndrome

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Retinitis Pigmentosa and Ataxia (NARP)

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
11
  • T Targeted variant analysis

NARP syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

NARP syndrome (neuropathy, ataxia and retinitis pigmentosa): Mutation analysis (T8993G)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • T Targeted variant analysis

mtSEEK® Mitochondrial Genome Sequencing with Deletion Detection and Heteroplasmy Analysis

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
1336
  • C Sequence analysis of the entire coding region

mtDNA common mutations panel

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
61
  • T Targeted variant analysis

Mitochondrial Genome Sequencing

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
61
  • C Sequence analysis of the entire coding region

Results: 1 to 14 of 14

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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