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Implementing Patch Clamp and Live Fluorescence Microscopy to Monitor Functional Properties of Freshly Isolated PKD Epithelium
Published on: September 1, 2015
Sunil Daga1, Victor Palit2, James A Forster3
1Consultant Nephrologist, St James's University Hospital, Leeds.
Cystinuria, an inherited kidney stone disease, results from amino acid reabsorption failure. Early diagnosis and specialized care are crucial for managing high recurrence rates and improving patient outcomes.
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