Disorders


 

HTRA2-Related Parkinson Disease


Synonym(s): PARK13, Parkinson Disease 13

 

OMIM

GeneLocusProtein
HTRA22p13.1 

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany• 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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