Disorders


 

CLCN2-Related Juvenile Myoclonic Epilepsy


 

OMIM

GeneLocusProtein
CLCN23q26-qterChloride channel protein 2

Laboratory Test Method Prenatal Carrier *
diagenos - Osnabrueck, Germany• Mutation scanning of the entire coding region
  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Medgene, MedGene - Bratislava, Slovakia  
Praxis fuer Humangenetik Wien - Vienna, Austria  

* 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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