A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM1 locus on chromosome 12

Creative Commons License

Sener E., Lee B., Turgut B., Akarsu A. N., Engle E.

ARCHIVES OF OPHTHALMOLOGY, cilt.118, sa.8, ss.1090-1097, 2000 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 118 Sayı: 8
  • Basım Tarihi: 2000
  • Doi Numarası: 10.1001/archopht.118.8.1090
  • Dergi Adı: ARCHIVES OF OPHTHALMOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1090-1097
  • Hacettepe Üniversitesi Adresli: Evet

Özet

Objectives: To describe the phenotype of a Turkish family with variably expressed congenital fibrosis of the extraocular muscles (CFEOM), and to determine the genetic location of their disorder.