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Results: 1 to 20 of 28

Tests names and labsConditionsGenes, analytes, and microbesMethods

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
123129
  • E Sequence analysis of select exons

PGmito - Mitochondrial Genome Sequencing

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

mtDNA - mitochondriopathy (MERRF)

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

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

Ataxia Exome

Genetic Services Laboratory University of Chicago
United States
289481
  • C Sequence analysis of the entire coding region

MERRF Syndrome (A8344G, T8356C, G8363A and G8361A) Analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

MERRF Syndrome (A8344G)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

mtDNA Targeted Analysis: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

mtDNA Targeted Analysis with Heteroplasmy: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

Common 29 mtDNA Variant Panel

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

Expanded 93 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • 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

Hearing Loss Advanced Sequencing and CNV Evaluation

Athena Diagnostics Inc
United States
249184
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MERRF SYNDROME

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

MERRF syndrome

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

mtDNA encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
1137
  • C Sequence analysis of the entire coding region

MERRF, MT-TK sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • C Sequence analysis of the entire coding region

MERRF Test

Genetics Laboratory - Department of Pathology Rush University Medical Center
United States
11
  • X Mutation scanning of select exons

Myoclonic epilepsy with red ragged fibers

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

Results: 1 to 20 of 28

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.