Disorders


 

Amyloidosis V


Synonym(s): Finnish Type Amyloidosis

 

OMIM

GeneLocusProtein
GSN9q33Gelsolin

Laboratory Test Method Prenatal Carrier *
HUSLAB, Laboratory of Genetics - Helsinki, Finland• Targeted mutation analysis
  
Mayo Clinic - Minnesota, Molecular Genetics Laboratory - Rochester, MN, 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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