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Genetic analysis of low magnesium
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创建时间：
2019-05-08
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Clinical and genetic features of the Fabry patients.
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711a6bc0-44ca-4078-b677-009d3cd84112 - samples
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Supplementary Material for: Detailed Assessment of Renal Function in a Proband with Harboyan Syndrome Caused by a Novel Homozygous SLC4A11 Nonsense Mutation
Background/Aims: To identify the underlying molecular genetic cause of disease in a patient with Harboyan syndrome and to perform a detailed assessment of her renal function. We also assessed the infl
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