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

