Associated Papers
Complex phenotype in Fanconi renotubular syndrome type 1: Hypophosphatemic rickets as the predominant presentation.
Li CY et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2024
Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia.
Ragate DC et al.
Journal of Bone and Mineral Metabolism, 2024
Association of Familial Fanconi Syndrome with a Novel GATM Variant.
Kudo H et al.
The Tohoku Journal of Experimental Medicine, 2023
A novel variant in GATM causes idiopathic renal Fanconi syndrome and predicts progression to end-stage kidney disease.
Seaby EG et al.
Clinical Genetics, 2023
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.
Reichold M et al.
Journal of the American Society of Nephrology : Jasn, 2018
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