Disorders


 

Congenital Stationary Night Blindness, Type 1D


 

OMIM

GeneLocusProtein
SLC24A115q22.31Sodium/potassium/calcium exchanger 1

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.

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