Disorders


 

SEPN1-Related Congenital Fiber-Type Disproportion


 

OMIM

GeneLocusProtein
SEPN11p36.13Selenoprotein N

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany  
Cologne University, Institute of Human Genetics - Cologne, Germany  
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA  
GSTS Pathology, DNA Laboratory - London, Great Britain  
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, 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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