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Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease.
Chou, Janice Y; Mansfield, Brian C.
Affiliation
  • Chou JY; Section on Cellular Differentiation, Heritable Disorders Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-1830, USA. chouja@mail.nih.gov
Hum Mutat ; 29(7): 921-30, 2008 Jul.
Article in En | MEDLINE | ID: mdl-18449899
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type I / Glucose-6-Phosphatase Type of study: Etiology_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2008 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type I / Glucose-6-Phosphatase Type of study: Etiology_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2008 Type: Article Affiliation country: United States