Disorders


 

SCN9A-Related Dravet Syndrome


 

OMIM

GeneLocusProtein
SCN9A2q24Sodium channel protein type 9 subunit alpha

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany• Sequence analysis of the entire coding region
  
Medical Neurogenetics - Atlanta, GA, USA• Sequence analysis of the entire coding region
  
Transgenomic - New Haven, CT, USA• Sequence analysis of the entire coding region
  

* 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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