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, vol.17, no.1, pp.359, 2022 (SCI-Expanded, Scopus)

  • Publication Type: Article / Article
  • Volume: 17 Issue: 1
  • Publication Date: 2022
  • Doi Number: 10.1186/s13023-022-02483-7
  • Journal Name: Orphanet journal of rare diseases
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, CINAHL, EMBASE, MEDLINE, Directory of Open Access Journals
  • Page Numbers: pp.359
  • Istanbul University Affiliated: Yes