EOSAL-LDLR

Seqplexing

Delivery time

3 weeks

Sample

Blood

215,00€

CNVs (large deletions and duplications, greater than 100 bp) in this gene cause up to 10% of cases of familial hypercholesterolemia caused by mutations in the LDLR gene. CNVs present in the LDLR gene (familial hypercholesterolemia). For blood or DNA swab samples.

Other tests

9-gene analysis using NGS - Familial hypercholesterolemia

9-gene analysis using NGS - Familial hypercholesterolemia

850,00€

Neurofibromatosis Test Complete sequencing of the SMARCB1 gene

Neurofibromatosis Test Complete sequencing of the SMARCB1 gene

586,85€

Test Neurofibromatosis genes (SMARCB1 and LZTR1)

Test Neurofibromatosis genes (SMARCB1 and LZTR1)

645,00€