gdmw | 59555
Morbus Wilson, H1069Q Mutation
Keywords
ATP7B, H1069Q
| Material |
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| Note |
ATP7B Mutation p.H1069Q. Diese Mutation kommt in 40% aller mitteleuropäischen Patienten vor. Analyse des kompletten Gens: Analysencode ngsmwi (=ATP7B Komplettsequenzierung). |
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| Min. quantity | 4 mL | |
| Stability | 1 week / 2-8°C | |
| Duration | 2 days | |
| Frequency | 1 x per week (thursday) | |
| Method | Polymerase Chain Reaction (PCR) / Sequenzing | |
| Price | CHF 0.00 | |
| Tariff | 0.00 TP |
Team of consultants
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PhD
Christoph Noppen
FAMH Specialist in laboratory medicine, medical genetics
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FAMH Specialist in laboratory medicine, medical genetics | T |
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DSc
Henriette Kurth
FAMH Specialist in laboratory medicine, medical genetics
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FAMH Specialist in laboratory medicine, medical genetics | T |
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Dr. sc. nat.
Andrea Salzmann
Candidate FAMH Specialist in laboratory medicine, main field medical genetics
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Candidate FAMH Specialist in laboratory medicine, main field medical genetics | T |
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