Article

Detection of Alport gene variants in children and young people with persistent haematuria

2023-11-08

Abstract excerpt

<title>Abstract</title> <p>Background Genetic kidney disease is an important cause of persistent microscopic haematuria in children and young people. We aimed to determine the frequency of variants in the Alport syndrome genes (<italic>COL4A3</italic>, <italic>COL4A4</italic> or <italic>COL4A5</italic>) in individuals under 18 years of age presenting with persistent microscopic haematuria to a single specialist...

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Literature Corpus work: 0161dc5b-0b9c-5327-b840-885bfe95c8dd
DOI: 10.21203/rs.3.rs-3539103/v1

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