Ophthalmology Panel
Ophthalmology Panel
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The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major ophthalmologic conditions
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 235 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Ceroid Lipofuscinosis
- Bardet-Biedl Syndrome
- Brown-Vialetto-Van Laere Syndrome
- Joubert Syndrome and Meckel Syndrome

Questo prodotto è destinato esclusivamente ai clienti che hanno già acquistato un test MyGenome