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gdmw | 59555

Morbus Wilson, H1069Q Mutation

Keywords:
ATP7B
H1069Q

Status

Material
Blood EDTA EDTA tube, purple (6)
Hint
ATP7B Mutation p.H1069Q. Diese Mutation kommt in 40% aller mitteleuropäischen Patienten vor. Analyse des kompletten Gens: Analysencode ngsmwi (=ATP7B Komplettsequenzierung).
Min. volume 4 mL
Stability
Stability
1 week / 2-8°C
Duration 2 days
Frequency 1 x per week (thursday)
Method Polymerase Chain Reaction (PCR) with hybridization

Price/Rate

Price
Price
CHF 0.00
Rate
Rate
0.00 TP