Disorders


 

Hereditary Folate Malabsorption


Synonym(s): Congenital Folate Malabsorption

 

GeneReviewOMIM

GeneLocusProtein
SLC46A117q11.2Proton-coupled folate transporter

Laboratory Test Method Prenatal Carrier *
General University Hospital in Prague, Institute of Inherited Metabolic Disorders - Praha, Czech Republic• 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...