GLUCOSE/GALACTOSE MALABSORPTION (SLC5A1) GENE SEQ

A genetic test to identify mutations in the SLC5A1 gene. This test is used to diagnose glucose/galactose malabsorption, a rare metabolic disorder.

Also known asGlucose/galactose Malabsorption (slc5a1) Gene Sequencing Glucose/galactose Malabsorption (slc5a1) Gene Sequencing

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
GLUCOSE/GALACTOSE MALABSORPTION (SLC5A1) GENE SEQ includes 1 parameter

  • Specimen

Test code

G675

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Others (fx)Others2 ML

Specimen stability information

Others (Fx)

Specimen rejection criteria

Test run frequency

Every Day TIME - 10:00

Turn around time

28 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

GLUCOSE/GALACTOSE MALABSORPTION (SLC5A1) GENE SEQ

22000