Functional analysis of compound heterozygous variations in the CLCNKB gene in a patient with Bartter syndrome type Ⅲ
ObjectiveTo explore the functional characteristics of a patient of Bartter syndrome type III and compound heterozygous mutations in CLCNKB gene and explore the rescue effect of cystic fibrosis transmembrane conductance regulator modulator compound VX-809 on CLCNKB gene missense variant.MethodsA retr...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Editorial Department of Journal of Clinical Nephrology,
2024-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |