Dear Colleagues,   We are happy to include your patient in our mutation analysis in single-gene causes of nephrotic syndrome.   Please inform the patient/parents that this process may take more than 6 months. If you do not hear from us that means we have not found the disease-causing mutation. In case we find the disease-causing mutation we may help you initiate CLIA-certified mutation analysis.   We will provide free shipment for the blood samples. To get started, please follow the instructions below.   Thank you for your interest! |   |
Disease |
Genes |
Paperwork/Unterlagen |
Nephrotic Syndrome |
NPHS1
NPHS2 WT1 PLCE1 LAMB2 CUBN INF2 COQ2 COQ6 ACTN4 SMARCAL1 MYO1E PDSS2 CD2AP PTPRO/GLEPP1 CFH SCARB2 NEIL1 TRPC6 LMX1B ITGA3 |
I have not completed CITI-Training: "How-to manual - PDF document"   I have completed CITI-Training: Please contact Shazia Ashraf   If you are an enrolled collaborator, please click here   If you are an enrolled collaborator and the participant is a non-English speaker, please click here   |
Last update on May, 2019