A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome

Biochemistry, Genetics and Molecular Biology

• Autosomal Recessive Inheritance 100%
• Cell Membrane 100%
• Cotransporter 100%
• Genetics 100%
• Loss of Function Mutation 100%
• Opossum 100%
• Rickets 100%
• Xenopus laevis 100%

Keyphrases

• Autosomal Recessive 20%
• Causative mutation 20%
• Consanguineous Family 20%
• Fanconi Syndrome 20%
• Frame Duplication 20%
• Functional Studies 20%
• Gain-of-function mutation 100%
• Genetic Analysis 20%
• Hypophosphatemic Rickets 20%
• Inorganic Phosphate 20%
• Loss Function 20%
• NaPi-IIa 100%
• Opossum Kidney Cells 20%
• Phosphate 40%
• Phosphate Cotransporter 20%
• Plasma Membrane 20%
• Proximal Tubule 20%
• Reabsorption 20%
• Renal Fanconi Syndrome 100%
• SLC34A1 20%
• Sodium 20%
• Xenopus Oocytes 20%

Medicine and Dentistry

• Autosomal Recessive Inheritance 50%
• Cell Membrane 50%
• Fanconi Syndrome 100%
• Genetic Analysis 50%
• Hypophosphatemic Rickets 50%
• Kidney Cell 50%
• Loss of Function Mutation 100%
• Oocyte 50%
• Sodium Phosphate Cotransporter 50%