Molecular Testing for Thalassemia: Mutation Detection According to Referral Reasons and Demographic Data

Creative Commons License

ALTINER Ş., KARABULUT H. G., EKİNCİ S., Vicdan A., KUTLAY N., TUNCALI T., ...Daha Fazla

ERCIYES MEDICAL JOURNAL, cilt.43, sa.5, ss.449-451, 2021 (ESCI) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 43 Sayı: 5
  • Basım Tarihi: 2021
  • Doi Numarası: 10.14744/etd.2021.95226
  • Dergi Adı: ERCIYES MEDICAL JOURNAL
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Academic Search Premier, CAB Abstracts, EMBASE, Veterinary Science Database, Directory of Open Access Journals, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.449-451
  • Anahtar Kelimeler: Thalassemia, Turkey, referral reason, mutation
  • Ankara Üniversitesi Adresli: Evet

Özet

Objective: Thalassemia is the most common inherited blood disorder worldwide and an important public health problem in Mediterranean countries such as Turkey. In this study, we aimed to define mutation detection rates according to referral reasons based on molecular testing results.