U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 21 to 30 of 30

Tests names and labsConditionsGenes, analytes, and microbesMethods

mtDNA Depletion/Integrity Panel (MitomeNGS)

Baylor Genetics
United States
2215
  • C Sequence analysis of the entire coding region

Mitochondrial genome sequencing

Molecular Vision Laboratory
United States
526339
  • C Sequence analysis of the entire coding region

Mitochondrial DNA depletion syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1815
  • C Sequence analysis of the entire coding region

Neuromuscular Disorders NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
233144
  • C Sequence analysis of the entire coding region

Mitochondrial Depletion NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
3223
  • C Sequence analysis of the entire coding region

Mitochondrial DNA Depletion Syndrome Panel

Blueprint Genetics
Finland
1025
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing MGME1

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

Nuclear encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
37302
  • C Sequence analysis of the entire coding region

Mitochondrial Diseases (mtDNA and 217 nuclear genes)

Asper Biogene Asper Biogene LLC
Estonia
89210
  • C Sequence analysis of the entire coding region

MGME1

MGZ Medical Genetics Center
Germany
31
  • C Sequence analysis of the entire coding region

Results: 21 to 30 of 30

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.