Gitelman syndrome – A new mutation in the SLC12A3 gene

類似資料

• Novel Intronic Mutations of the SLC12A3 Gene in Patients with Gitelman Syndrome
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  出版事項: (2023-05-01)
• Research Analysis of SLC12A3 Gene Mutation and Molecular Mechanism in Gitelman Syndrome
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• A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene
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• Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome
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