Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Wenn gleichzeitig eine Mutation des Chloridkanals B (CLCNKB) vorliegt, so können Mutationen des CLCNKA-Gens das autosomal rezessive infantile Bartter -Syndrom auslösen.
| Clinic | Method | Familienuntersuchung |
| Turnaround | 5 days | |
| Specimen type | genomic DNA |
| Clinic | Method | Hochdurchsatz-Sequenzierung |
| Turnaround | 25 days | |
| Specimen type | genomic DNA |
| Clinic | Method | Direkte Sequenzierung der proteinkodierenden Bereiche eines Gens |
| Turnaround | 25 days | |
| Specimen type | genomic DNA |
| Clinic | Method | Multiplex ligationsabhängige Amplifikation |
| Turnaround | 20 days | |
| Specimen type | genomic DNA |
 |
Copyright © 2005-2020 by Center for Nephrology and Metabolic Disorders, Dr. Mato Nagel, MD Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Germany, Tel.: +49-3576-287922, Fax: +49-3576-287944 Sitemap | Webmail | Disclaimer | Privacy Issues |
