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Condition



Test Name

Hereditary Hemolytic Anemia Panel (For RBC membrane disorders and Enzymopathies)[Expedited TAT]

Inclusive Genes



ABCG5, ABCG8, AK1, ALDOA, ANK1, C15orf41, CDAN1, EPB41, EPB42, G6PD, GATA1, GCLC, GPI, GPX1, GSR, GSS, HK1, KIF23, KLF1, NT5C3A, PIEZO1, PKLR, RHAG, SEC23B, SLC4A1, SPTA1, SPTB, TPI1

Specimen Type

Peripheral blood/purified genomic DNA/chorionic villus sample (CVS)/Amniotic Fluid

Container

Transportation Temperature

20-25⁰C CVS at 2-8⁰C

Volume

Minimum 3ml of peripheral blood; minimum 1 microgram of DNA (concentration of 50-100ng/microliters); 300-500mg of CVS; Amniotic fluid of 15-20ml/T25 culture flask with 100% confluency

Methodology

Next Generation Sequencing

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