HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Prevalence of myocilin and optineurin sequence variants in German normal tension glaucoma patients.

AbstractPURPOSE:
To determine the prevalence of optineurin (OPTN) and myocilin (MYOC) sequence variants in a cohort of German patients with normal tension glaucoma.
METHODS:
All coding exons of the OPTN and MYOC genes were amplified by PCR from genomic DNA and subjected to direct DNA sequencing. Analysis of sequence variants in controls was done by denaturing high performance liquid chromatography (DHPLC) and restriction fragment length polymorphism (RFLP) analysis.
RESULTS:
Sequence variants were identified by DNA sequencing in 10 of 112 cases. The OPTN sequence variant M98K was found in seven patients. In addition, two novel sequence variants (A336G and A377T) in the OPTN gene were identified that were not present in a control group. Mutation screening also identified two potentially pathogenic MYOC mutations (T293K and A445V).
CONCLUSIONS:
The findings in the current study provide further evidence that MYOC and OPTN gene variants are rare causes of NTG.
AuthorsNicole Weisschuh, Dorit Neumann, Christiane Wolf, Bernd Wissinger, Eugen Gramer
JournalMolecular vision (Mol Vis) Vol. 11 Pg. 284-7 (Apr 18 2005) ISSN: 1090-0535 [Electronic] United States
PMID15851979 (Publication Type: Journal Article)
Chemical References
  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • Eye Proteins
  • Glycoproteins
  • Membrane Transport Proteins
  • OPTN protein, human
  • Transcription Factor TFIIIA
  • Untranslated Regions
  • trabecular meshwork-induced glucocorticoid response protein
Topics
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Cell Cycle Proteins
  • Chromatography, High Pressure Liquid
  • Cytoskeletal Proteins (genetics)
  • Eye Proteins (genetics)
  • Female
  • Genetic Variation
  • Germany (epidemiology)
  • Glaucoma, Open-Angle (ethnology, genetics)
  • Glycoproteins (genetics)
  • Humans
  • Introns (genetics)
  • Male
  • Membrane Transport Proteins
  • Middle Aged
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Prevalence
  • Sequence Analysis, DNA
  • Transcription Factor TFIIIA (genetics)
  • Untranslated Regions (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: