Disorders


 

Congenital Stationary Night Blindness, Type 1F


 

OMIM

GeneLocusProtein
LRIT34q25Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3

Laboratory Test Method Prenatal Carrier *
Oregon Health and Science University, Casey Eye Institute Molecular Diagnostic Laboratory - Portland, OR, USA  

* 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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