Correction: Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant

Eur J Hum Genet. 2024 Nov 25. doi: 10.1038/s41431-024-01736-2. Online ahead of print.

Sergio Daga^#^{1

2}, Lorenzo Loberti^#^{1

2

3}, Giulia Rollo^{1

2}, Loredaria Adamo^{1

2}, Olga Lorenza Colavecchio³, Giulia Brunelli^{1

2

4}, Kristina Zguro^{1

2}, Sergio Antonio Tripodi⁵, Andrea Guarnieri⁶, Guido Garosi⁶, Romina D'Aurizio⁴, Francesca Ariani^{1

2

3}, Rossella Tita³, Alessandra Renieri^{7

8

9}, Anna Maria Pinto¹⁰

¹ Medical Genetics, University of Siena, Siena, Italy.
² Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.
³ Genetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
⁴ Institute of Informatics and Telematics, CNR, Pisa, Italy.
⁵ Department of Pathology, AOUS, Siena, Italy.
⁶ Department of Medical Sciences, Nephrology, Dialysis and Transplantation Unit, University Hospital of Siena, Siena, Italy.
⁷ Medical Genetics, University of Siena, Siena, Italy. [email protected].
⁸ Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy. [email protected].
⁹ Genetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy. [email protected].
¹⁰ Genetica Medica, Azienda Ospedaliero-Universitaria Senese, Siena, Italy. [email protected].

^# Contributed equally.

No abstract available

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