Disorders


 

Phosphoserine Aminotransferase Deficiency


 

OMIM

GeneLocusProtein
PSAT19q21.2Phosphoserine aminotransferase

Laboratory Test Method Prenatal Carrier *
University Medical Center Utrecht, Genome Diagnostics Laboratory - Utrecht, Netherlands• 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.

Loading...