Hereditary Hearing Loss: Usher Syndrome
|
|
|
Alternate Gene Names
USH3, USH3A, RP61, CIP98, WHRN, USH2D, PDZD7B, USH2C, MASS1, DKFZp761P0710, KIAA0686, FEB4, VLGR1b, USH1B, DFNB2, DFNA11, NSRD2, USH1F, DFNB23, CDHR15, PDZK7, FLJ23209, bA108L7.8, DFNB18, PDZ73, harmonin, NY-CO-37, NY-CO-38, PDZ-73, AIE-75, PDZD7C, Sans, FLJ33924, ANKS4A, USH2, RP39, DFNB12, USH1D, DFNB48, USH1J, CDHR23, KIP2, GPR98, DFNB31
Blood; please contact the Genome Diagnostics Laboratory if you want to send gDNA. If sending a prenatal sample, please contact the laboratory prior to sending sample to discuss sample requirements.
For details about specimen requirements, please refer to: Specimen Types & Requirements (PDF).
- Blood: 5-10 mL in EDTA, 0.5 mL in EDTA (neonate);
- DNA-minimum 10 ug in 100 uL low TE (pH8.0)
Blood-Room Temperature. Please contact the Genome Diagnostics Laboratory if you want to send gDNA.
If sample shipment >48 hours, ship on ice.
Special Instructions for Genome Diagnostics Samples
Please ship us the blood sample within 48 hours of collection.
Usher syndrome
Browse tests by laboratory
Customer Service
Toll Free: 1-855-381-3212
Local: 416-813-7200