Catalogue
CONGENITAL DISORDER OF GLYCOSYLATION TYPE IA (CDG1A) , SEQUENCING PMM2...
| Test Code |
35300 |
|---|---|
| Gene/s |
See all genes  Hide all genes  PMM2 |
| Analysis Methods |
Sanger Sequencing |
| Sample Requirements |
5 mL whole blood (EDTA). Necessary clinical and family history. |
| TAT |
30 days |
| Omim G |
601785 |
| Omim F |
212065 |
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Do you need more information?
Contact us at
genetics@referencelaboratory.es
Are you a verified customer?
Ordering a test or Service from
us is simple and quick
Check our sample requirements
We have optimized all our processes to accept a wide range of samples, always adapting to each case.