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Room temperature
Panel + CNV
Exome
Exome + CNV
Specific request form : Exome
"Whole Exome Sequencing" brochure
Hearing loss-familial salivary gland insensitivity to aldosterone syndrome
International Division
Monday-Friday :
8.30 am - 6.30 pm (GMT + 1)
T. : +33 4 72 80 23 85
Contact by email
8.30 am - 6.30 pm (GMT + 1)
T. : +33 4 72 80 23 85
Contact by email
Disease code:
ORPHA:3225Associated therapeutic area(s):
Abnormality of metabolism/homeostasis (HP:0001939)
Abnormality of head or neck (HP:0000152)
Abnormality of the ear (HP:0000598)
Abnormality of head or neck (HP:0000152)
Abnormality of the ear (HP:0000598)
Prenalytics:
5 mL whole blood or DNA sampleRoom temperature
Turnaround time:
4 semainesOptions available :
PanelPanel + CNV
Exome
Exome + CNV
Documents to download:
Specific request form: Rare diseasesSpecific request form : Exome
"Whole Exome Sequencing" brochure
Important
You have the possibility to add isolated genes in addition to your selection, directly on the test request form.
