NGS analysis - Familial cerebral small vessel disease

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GENE / VARIANT / LOCUS
ABCC6, ACTA2, ADA2, APP, COL3A1, COL4A1, COL4A2, CSF1R, CST3, CTC1, CTSA, FOXC1, GLA, GSN, HTRA1, ITM2B, NOTCH3, PRNP, TREX1
SPECIALIZATIONS
Neurology / neuropediatrics
Neurology / neuropediatrics
METHODOLOGY
TAT (DAYS)
365 calendar days
OMIM CODE (GENE/LOCUS)
OMIM CODE (FENOTYPE)
RefSNP ID
ACCREDITATION
No
SAMPLE REQUIREMENTS
Sample type Volume/Concentration1 Container Transport temperature Sample viability (days/hours)2
Peripheral blood ≥ 3 ml K3/K2 EDTA Room temp. 5
Peripheral blood 1 ml K3/K2 EDTA - newborn Room temp. 5
Peripheral blood 1 ml K3/K2 EDTA - newborn Room temp. 5
Peripheral blood ≥ 3 ml K3/K2 EDTA Room temp. 5

1 If it is not possible to collect the minimum volume for the test, please contact Unilabs Genetics

2 Maximum shipping time to ensure sample quality

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