Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy.

Dedeoglu S., Dede E., Oztunc F., Gedikbasi A., Yesil G., Dedeoglu R.

Orphanet journal of rare diseases, cilt.17, sa.1, ss.359, 2022 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 17 Sayı: 1
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1186/s13023-022-02483-7
  • Dergi Adı: Orphanet journal of rare diseases
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CINAHL, EMBASE, MEDLINE, Directory of Open Access Journals
  • Sayfa Sayıları: ss.359
  • İstanbul Üniversitesi Adresli: Evet