Your browser doesn't support javascript.
loading
Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.
Beyzaei, Zahra; Ezgu, Fatih; Geramizadeh, Bita; Alborzi, Alireza; Shojazadeh, Alireza.
Affiliation
  • Beyzaei Z; Shiraz Transplant Research Center (STRC), Shiraz University of Medical Sciences, Shiraz, Iran.
  • Ezgu F; Department of Pediatric Metabolism and Genetic, Gazi University Faculty of Medicine, Ankara, Turkey.
  • Geramizadeh B; Shiraz Transplant Research Center (STRC), Shiraz University of Medical Sciences, Shiraz, Iran. geramib@gmail.com.
  • Alborzi A; Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran. geramib@gmail.com.
  • Shojazadeh A; , Shiraz, Iran. geramib@gmail.com.
BMC Pediatr ; 21(1): 175, 2021 04 15.
Article in En | MEDLINE | ID: mdl-33858366
Subject(s)
Key words
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Glycogen Storage Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Female / Humans Country/Region as subject: Asia Language: En Year: 2021 Type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Glycogen Storage Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Female / Humans Country/Region as subject: Asia Language: En Year: 2021 Type: Article