Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type Ⅲ

• Amira Mili

• Ilhem Ben Charfeddine

• Ons Mamai

Journal

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 57 (3), 170-175, 2012-03

  Tokyo : Springer Nature

Keywords

• amylo-1,6-glucosidase
• AGL gene
• glycogen storage disease type Ⅲ
• haplotype analysis
• founder effect
• novel mutation

Details

• CRID: 1523669555121293184
• NII Article ID: 10030711965
• NII Book ID: AA11206160
• ISSN: 14345161
• NDL BIB ID: 023513804
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I023513804
• Web Site: https://search.jamas.or.jp/link/ui/2013000570
• Text Lang: en
• NDL Source Classification:
  • ZS16(科学技術--医学--人類遺伝学)
• Data Source:
  • NDL
  • CiNii Articles