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Results: 1 to 20 of 29 (representing 15 labs)

Tests names and labsConditionsGenes and analytesMethods

PLA2G6-Associated Neurodegeneration, Infantile Neuroaxonal Dystrophy and Parkinson Disease via the PLA2G6 Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Neurodegeneration with Brain Iron Accumulation and Infantile Neuroaxonal Dystrophy Sequencing Panel

PreventionGenetics
United States
1211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Neurodegeneration with Brain Iron Accumulation

Asper Biotech Asper Biotech Ltd.
Estonia
1010
  • C Sequence analysis of the entire coding region

Infantile Neuroaxonal Dystrophy (INAD), PLA2G6, Sequencing

NBIA Testing Center Oregon Health & Science University
United States
51
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy NGS Panel

Fulgent Genetics
United States
3052447
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurodegeneration with Brain Iron Accumulation Disorders

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
129
  • C Sequence analysis of the entire coding region

DYSTONIA

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1513
  • C Sequence analysis of the entire coding region

Dystonia

Asper Biotech Asper Biotech Ltd.
Estonia
3738
  • C Sequence analysis of the entire coding region

NGS panel - Neurodegeneration with brain iron accumulation

Genome Diagnostics VU University Medical Center
Netherlands
1110
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Neurodegeneration with Brain Iron Accumulation NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
179
  • C Sequence analysis of the entire coding region

PLA2G6 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • C Sequence analysis of the entire coding region

Single gene testing PLA2G6

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

Parkinson Disease, Early Onset NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
149
  • C Sequence analysis of the entire coding region

PLA2G6

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkinson-Alzheimer-Dementia NGS Panel

Fulgent Genetics
United States
8237
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
752392
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy NGS Panel

Fulgent Genetics
United States
597343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Infantile Neuroaxonal Dystrophy (INAD), PLA2G6, Sequencing and Deletion/Duplication

NBIA Testing Center Oregon Health & Science University
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Infantile Neuroaxonal Dystrophy (INAD), PLA2G6, Deletion/Duplication

NBIA Testing Center Oregon Health & Science University
United States
51
  • D Deletion/duplication analysis

Infantile Neuroaxonal Dystrophy (INAD), PLA2G6, Deletion/Duplication

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
41
  • D Deletion/duplication analysis

Results: 1 to 20 of 29

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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