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Aggressive therapy improves cirrhosis in glycogen storage disease type IX

  • Published:2013-06 Issue:2 Volume:109 Page:179-182
  • ISSN:1096-7192
  • Container-title:Molecular Genetics and Metabolism
  • language:en
  • Short-container-title:Molecular Genetics and Metabolism

Author:

Tsilianidis Laurie A.,Fiske Laurie M.,Siegel Sara,Lumpkin Chris,Hoyt Kate,Wasserstein Melissa,Weinstein David A.

Funder

National Institutes of Health (NIH)

National Center for Research Resources (NCRR)

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference14 articles.

1. Phosphorylase kinase deficiency of the liver: deficiency in a girl with increased hepatic glycogen;Hug;Science,1966

2. X-chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency;Huijing;Am. J. Hum. Genet.,1969

3. Severe phenotype of phosphorylase kinase-deficient liver glycogenosis with mutations in the PHKG2 gene;Burwinkel;Pediatr. Res.,2003

4. Detection of PHKA2 gene mutation in four Japanese patients with hepatic phosphorylase kinase deficiency;Ban;Tohoku J. Exp. Med.,2003

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