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
 

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Last update on July, 2017