The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14.

Benzer Materyaller

• Isolation and mapping of a polymorphic DNA sequence for human muscle glycogen phosphorylase (pMCMP1) on chromosome II [PYGM].
  Yazar:: Carlson, M, ve diğerleri
  Baskı/Yayın Bilgisi: (1988)
• Liver Glycogen Phosphorylase Deficiency Leads to Profibrogenic Phenotype in a Murine Model of Glycogen Storage Disease Type VI
  Yazar:: Lane H. Wilson, ve diğerleri
  Baskı/Yayın Bilgisi: (2019-11-01)
• Liver Glycogen Phosphorylase Deficiency Leads to Profibrogenic Phenotype in a Murine Model of Glycogen Storage Disease Type VI
  Yazar:: Wilson, Lane H., ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• Sequence analysis of the cDNA encoding human liver glycogen phosphorylase reveals tissue-specific codon usage.
  Yazar:: Newgard, C B, ve diğerleri
  Baskı/Yayın Bilgisi: (1986)
• Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
  Yazar:: Baqué, S, ve diğerleri
  Baskı/Yayın Bilgisi: (1994)