Myotonic dystrophy, type II (DM2)
| Genes (full coding region): |
CNBP |
| Lab method: | Sanger sequencing |
| TAT: | 2-4 weeks |
| Specimen requirements: | 2-4 ml of blood with anticoagulant EDTA
4 µg DNA in TE, AE or pure sterile water at 100-250 ng/µl |
| Ordering information: | Go to online ordering or download sample submission form |
Indications for genetic testing:
1. Confirmation of clinical diagnosis
2. Carrier testing for at-risk relatives
3. Genetic counseling

