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SAG Remaining Exon Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
SAG
Disorders:
Clinical Utility:
  • Confirmation of a clinical diagnosis.
  • Development of an appropriate management plan.
  • Prenatal diagnosis in families with a defined mutation
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
518
Turnaround Time:
6-7 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81479x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 368.61: Congenital night blindness, Hereditary night blindness, Oguchi's disease
  • 368.63: Abnormal dark adaptation curve, Abnormal threshold of cones or rods, Delayed adaptation of cones or rods
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. al-Jandal et al., (1999) Human Mutation 13:75-81
  2. Dryja et al., (1993) Nat Genet 4:280-283
  3. Yamamoto H et al., (1999) Nat Genet 22:188-91
  4. Nakamura et al. (2003) Doc Ophthalmol 107(1):3-11
  5. Nakamura et al., (2000) Invest Ophthalmol Vis Sci 41(12):3925-32
  6. Yamamoto et al., (1997) Nat Genet 15(2):175-178
  7. Nakamura et al., (2004) American Academy of Ophthalmology 111(7):1410-1414
  8. Nakazawa et al., (1998) Arch Ophthalmol 116:498-501
  9. Fuchs et al., (1995) Nat Genet 10:360-362
  10. Li et al., (2009) Am J Hum Genet 85:711-719
  11. Audo et al., (2009) Am J Hum Genet 85: 720- 729
  12. Bech-Hansen et al., (2000) Nat Genet 26: 319-323
  13. Pusch et al., (2000) Nat Genet 26:324-327
  14. Xiao et al., (2006) J Hum Genet 51:634-640
  15. van Genderen et al., (2009) Am J Hum Genet 85: 730-736

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