Disorders


 

Congenital Stationary Night Blindness, Type 1E


 

OMIM

GeneLocusProtein
GPR17917q21.1Probable G-protein coupled receptor 179

Laboratory Test Method Prenatal Carrier *
Oregon Health and Science University, Casey Eye Institute Molecular Diagnostic Laboratory - Portland, OR, USA• Sequence analysis of the entire coding region
• Deletion/duplication analysis

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

Loading...