GTR Home > Tests > Test for Congenital Stationary Night Blindness, Autosomal Dominant 3

Overview

Conditions for which test is offered: Congenital Stationary Night Blindness, Autosomal Dominant 3

Testing Method

  • Molecular Genetics
    • Sequence analysis of the entire coding region

Contact Policy Help

Pre-test email/phone consultation regarding genetic test utilization and decision making is provided to patients/families.
Post-test email/phone consultation regarding genetic test results and interpretation is provided to patients/families.

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.

Write to the Help Desk