Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Oxalat-Transporter SLC26A6

Der Oxalat-Transporter SLC26A6 is möglicherweise für das Syndrom der Hyperoxalurie mit Diarrhoe verantwortlich sein.

Genetests:

Research 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

Related Diseases:

Nephrolithiasis-Diarrhoe-Syndrom
SLC26A6
Update:
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