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Results: 1 to 17 of 17

Tests names and labsConditionsGenes, analytes, and microbesMethods

Supranuclear palsy, progressive, 601104, Autosomal dominant; PSNP1 (Progressive supranuclear palsy) (MAPT gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Supranuclear palsy, progressive, 601104, Autosomal dominant; PSNP1 (Progressive supranuclear palsy) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Frontotemporal Dementia via the MAPT Gene

PreventionGenetics, part of Exact Sciences
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Frontotemporal Dementia With Parkinsonism-17 (MAPT Single Gene Test)

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Progressive Supranuclear Palsy (MAPT Single Gene Test)

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MAPT-Related Disorders: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
51
  • C Sequence analysis of the entire coding region

PROGRESSIVE SUPRANUCLEAR PALSY

Laboratorio de Genetica Clinica SL
Spain
21
  • C Sequence analysis of the entire coding region

Classic Progressive Supranuclear Palsy , Sequencing MAPT Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing MAPT

CeGaT GmbH
Germany
41
  • C Sequence analysis of the entire coding region

MAPT Single Gene

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FTD - ALS panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2815
  • C Sequence analysis of the entire coding region

Parkinson-Alzheimer-Dementia NGS Panel

Fulgent Genetics
United States
7739
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis NGS Panel

Fulgent Genetics
United States
8443
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Supranuclear palsy, progressive

MedGene
Slovakia
11
  • E Sequence analysis of select exons

Supranuclear palsy, progressive

Praxis fuer Humangenetik Wien
Austria
11
  • E Sequence analysis of select exons

Test for MAPT-Related Disorders

Secugen SL
Spain
11
  • C Sequence analysis of the entire coding region

Results: 1 to 17 of 17

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.