Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease

Author： Kishnani Priya S.   Chuang Tzu-Po   Bali Deeksha   Koeberl Dwight   Austin Stephanie   Weinstein David A.   Murphy Elaine   Chen Ying-Ting   Boyette Keri   Liu Chu-Hao   Chen Yuan-Tsong   Li Ling-Hui  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.18, Iss.24, 2009-12, pp. : 4781-4790

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Sustained hepatic and renal glucose-6-phosphatase expression corrects glycogen storage disease type Ia in mice

By Sun M-S.  

Human Molecular Genetics, Vol. 11, Iss. 18, 2002-06 ,pp. : 2155-2164

Oxford University Press

Access to resources Recommend Favorite

Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VI

By Chang S.  

Human Molecular Genetics, Vol. 7, Iss. 5, 1998-05 ,pp. : 865-870

Oxford University Press

Access to resources Recommend Favorite

Human acid α -glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II

By Bijvoet Agnes G. A.  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2145-2153

Oxford University Press

Access to resources Recommend Favorite

Evidence for a Founder Effect in Sicilian Patients with Glycogen Storage Disease Type II

By  

Human Heredity, Vol. 50, Iss. 6, 2000-07 ,pp. : 331-333

Karger

Access to resources Recommend Favorite

Glycogen Storage Disease Type II: Birth Prevalence Agrees with Predicted Genotype Frequency

By  

Public Health Genomics, Vol. 2, Iss. 2-3, 2000-03 ,pp. : 91-96

Karger

Access to resources Recommend Favorite