HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A unique form of autosomal dominant cataract explained by gene conversion between beta-crystallin B2 and its pseudogene.

Authors Vanita, V Sarhadi, A Reis, M Jung, D Singh, K Sperling, J R Singh, J Bürger
JournalJournal of medical genetics (J Med Genet) Vol. 38 Issue 6 Pg. 392-6 (Jun 2001) ISSN: 1468-6244 [Electronic] England
PMID11424921 (Publication Type: Letter, Research Support, Non-U.S. Gov't)
Chemical References
  • Crystallins
Topics
  • Base Sequence
  • Cataract (genetics, pathology)
  • Child
  • Crystallins (genetics)
  • Family Health
  • Female
  • Gene Conversion
  • Genes, Dominant
  • Genetic Variation
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation
  • Pedigree
  • Phenotype
  • Pseudogenes
  • Sequence Homology, Nucleic Acid

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: