Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum

Overview of attention for article published in Orphanet Journal of Rare Diseases, March 2023

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Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum https://t.co/ZuZEFd2rU5 https://t.co/SNeBHcD8us

14 Mar 2023

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Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum https://t.co/gBc24YWhPV

13 Mar 2023

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