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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

PLA2G6-Associated Neurodegeneration: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
31
  • C Sequence analysis of the entire coding region

Infantile Neuroaxonal Dystrophy, PLA2G6, Sequencing

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
41
  • 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

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 & Science University
United States
41
  • D Deletion/duplication analysis

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

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
41
  • M Methylation analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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.