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Response to "Diagnose autosomal recessive Alport syndrome in an m.3243A>G carrier only if a pathogenic COL4A3 variant

Takaya Sasaki1,2, Daisuke Nakashima1,2, Takeshi Tosaki1,2

  • 1Division of Nephrology and Hypertension, Department of Internal Medicine, The Jikei University School of Medicine, Japan.

Internal Medicine (Tokyo, Japan)
|September 3, 2025
PubMed
Abstract

No abstract available in PubMed .

Keywords:
MELASautosomal dominant Alport syndromemitochondrial disease

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