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Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects.
- Published in:
- Biomedicines, 2021, v. 9, n. 7, p. 788, doi. 10.3390/biomedicines9070788
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- Article
An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro‐Asian stone‐forming belt.
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- Journal of Inherited Metabolic Disease Reports, 2020, v. 51, n. 1, p. 45, doi. 10.1002/jmd2.12077
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- Article
Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria.
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- Metabolomics, 2012, v. 8, n. 5, p. 951, doi. 10.1007/s11306-011-0391-3
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- Article
Predictors for poststroke outcomes: the Tel Aviv Brain Acute Stroke Cohort (TABASCO) study protocol.
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- International Journal of Stroke, 2012, v. 7, n. 4, p. 341, doi. 10.1111/j.1747-4949.2011.00652.x
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- Article
Current strategy for genetic analysis of haemophilia A families.
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- Haemophilia, 1996, v. 2, n. 1, p. 11, doi. 10.1111/j.1365-2516.1996.tb00003.x
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- Article