Characterization of the mutations in the glucose‐6‐phosphatase gene in Israeli patients with glycogen storage disease type 1a: R83C in six Jews and a novel V166G mutation in a Muslim Arab

Overview of attention for article published in Journal of Inherited Metabolic Disease, September 1994

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Article in Orphanet Journal of Rare Diseases (November 2020)

Preprint in Research Square (October 2020)

Article in Genetics and Molecular Biology (November 2013)

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