Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases

Overview of attention for article published in Orphanet Journal of Rare Diseases, September 2022

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Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases https://t.co/o00UqqkBCl

06 Nov 2022

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@rareireland

25 Sep 2022

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Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases https://t.co/bIBvf7kKqb

25 Sep 2022

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