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Results: 1 to 20 of 56 (representing 34 labs)

Tests names and labsConditionsGenes and analytesMethods

Leber Hereditary Optic Neuropathy

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
10
  • T Targeted variant analysis

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-ND1, MT-ND6, MT-ND4. Detection of the mutations m.11778G>A, m.14484T>C and m.3460G>A by sequencing

Instituto de Medicina Genomica
Spain
13
  • E Sequence analysis of select exons

MTND1, MTND4, MTND6. Detection of the mutations m.11778G>A, m.14484T>C y m.3460G>A by sequencing

Instituto de Medicina Genomica
Spain
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

Leber Hereditary Optic Neuropathy

Molecular Genetics and Cytogenetics, Clinical Laboratory Service Faculty of Medicine, Pontificia Universidad Católica de Chile
Chile
13
  • T Targeted variant analysis

Leber's Hereditary Optic Neuropathy

Molecular Pathology Laboratory Ohio State University
United States
11
  • T Targeted variant analysis

LEBER HEREDITARY OPTIC NEUROPATHY (LHON)

Laboratorio de Genetica Clinica SL
Spain
112
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

LEBER HEREDITARY OPTIC NEUROPATHY (LHON)

Laboratorio de Genetica Clinica SL
Spain
112
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary optic neuropathy, including Leber's hereditary optic neuropathy (NGS panel of 5 genes and 3 frequent mutations on mt DNA)

CGC Genetics
Portugal
78
  • C Sequence analysis of the entire coding region

Hereditary optic neuropathy, including Leber's hereditary optic neuropathy (NGS panel of 5 genes and 3 frequent mutations on mt DNA)

CGC Genetics
Portugal
78
  • C Sequence analysis of the entire coding region

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

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

LHON - 3 mutation( G3460A, G11778A, T14484C)

Diagnostics Division Centre for DNA Fingerprinting and Diagnostics
India
11
  • E Sequence analysis of select exons

Leber hereditary optic neuropathy

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

Single gene testing MT-ND6

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Single gene testing MT-ND4

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Single gene testing MT-ND1

CeGaT GmbH
Germany
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 MTCO3 gene)

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

Leber congenital neuropathy (sequence analysis of MTCYB)

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

Results: 1 to 20 of 56

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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