Filters

See more specimen types...

Other countries

See more countries

Results: 1 to 20 of 55

Tests names and labsConditionsGenes, analytes, and microbesMethods

Mitochondrial Genome Sequencing and Depletion/Integrity Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4752
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Leber Hereditary Optic Neuropathy (LHON)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
13
  • T Targeted variant analysis

PGmito - Mitochondrial Genome Sequencing

PreventionGenetics
United States
1638
  • C Sequence analysis of the entire coding region

mtDNA - mitochondriopathy (Leber)

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

Leber optic atrophy panel

Amplexa Genetics Amplexa Genetics A/S
Denmark
18
  • S Mutation scanning of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
342268
  • C Sequence analysis of the entire coding region

Leber hereditary optic atrophy(LHON): 3 mutations(G3460A, G11778A, T14484C)

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
13
  • T Targeted variant analysis

Leber's Hereditary Optic Neuropathy

Molecular Genetics Laboratory London Health Sciences Centre
Canada
13
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

LHON Gene Analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
13
  • T Targeted variant analysis

Leber hereditary optic neuropathy (LHON) mutation analysis

Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center
Turkey
11
  • C Sequence analysis of the entire coding region

Targeted mtDNA Analysis: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1127
  • T Targeted variant analysis

Targeted mtDNA Analysis with Heteroplasmy: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1127
  • T Targeted variant analysis

Common 29 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
917
  • T Targeted variant analysis

Expanded 93 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1127
  • T Targeted variant analysis

Leber optic atrophy (sequence analysis of MTND1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leber optic atrophy (sequence analysis of MTCO1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leber optic atrophy (sequence analysis of MTND5 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leber optic atrophy (sequence analysis of MTND2 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leber optic atrophy (sequence analysis of MTCO3 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leber congenital neuropathy (sequence analysis of MTCYB gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 55

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.

Support Center