Identification of fibrillin gene defects in Marfan Syndromeand ectopia lentis

  • Farndon, Peter (Principal Investigator)

Project Details

Short titleIdentification of fibrillin gene defects in Marfan Syndromeand ectopia lentis
StatusFinished
Effective start/end date1/11/92 → 31/10/95

Funding

  • UHB CHARITABLE FUNDS