Disorders


 

CHRNB2-Related Nocturnal Frontal Lobe Epilepsy, Autosomal Dominant


Synonym(s): ADNFLE Type 3, Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 3, CHRNB2-Related ADNFLE

 

OMIM

GeneLocusProtein
CHRNB21q21.3Neuronal acetylcholine receptor subunit beta-2

Laboratory Test Method Prenatal Carrier *
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA• Sequence analysis of the entire coding region
  
CeGaT GmbH - Tuebingen, Germany• Sequence analysis of the entire coding region
  
Centogene AG, Rare Disease Company - Rostock, Germany• Sequence analysis of the entire coding region
• Deletion/duplication analysis
 
diagenos - Osnabrueck, Germany• Sequence analysis of the entire coding region
 
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel• Sequence analysis of the entire coding region
 
Ludwig-Maximilians University Munich, Institute of Human Genetics - Munich, Germany• Sequence analysis of select exons
 
Medgene, MedGene - Bratislava, Slovakia• Sequence analysis of the entire coding region
 
Praxis fuer Humangenetik Wien - Vienna, Austria• 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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