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Alport syndrome is a genetic disorder affecting the basement membranes of the kidney, ear and eye, and represents a leading cause of monogenic kidney disease. Alport syndrome is genetically heterogeneous with three key genes involved (COL4A3‐5) and several transmission patterns, including monogenic X‐linked, autosomal recessive/dominant and digenic. We report a consanguineous family where 13 individuals...
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