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Results: 1 to 16 of 16

Tests names and labsConditionsGenes, analytes, and microbesMethods

Mitochondrial Genome Sequencing and Depletion/Integrity Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4852
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Combined mtDNA+Nuclear Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
12221
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Mitochondrial Full Genome Analysis

Mayo Clinic Laboratories Mayo Clinic
United States
2937
  • C Sequence analysis of the entire coding region

PGmito - Mitochondrial Genome Sequencing

PreventionGenetics, part of Exact Sciences
United States
1638
  • C Sequence analysis of the entire coding region

mtDNA - mitochondriopathy (NARP)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

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

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
126
  • 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

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
427
  • T Targeted variant analysis

Neuromuscular Disorders Panel 

CGC Genetics Unilabs
Portugal
17367
  • C Sequence analysis of the entire coding region

Mitochondrial Disorders Panel

Dhiti Omics Technologies Private Ltd
India
2837
  • C Sequence analysis of the entire coding region

Common 29 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
932
  • T Targeted variant analysis

Mito Genome Sequencing & Deletion Testing

GeneDx
United States
2438
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NEUROPATHY, ATAXIA Y RETINITIS PIGMENTOSA (NARP)

Laboratorio de Genetica Clinica SL
Spain
11
  • X Mutation scanning of select exons

Hearing Loss NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
198157
  • C Sequence analysis of the entire coding region

NARP syndrome

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

NARP syndrome

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

NARP syndrome

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

Results: 1 to 16 of 16

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