Phenotype and genotype analyses of 21 Chinese patients with Dent disease. [PDF]
Che R, Cai Y, Zhou W, Zhao S, Huang S.
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Prenatal Ultrasound Diagnosis and Prognosis Analysis of Fetal Congenital Cataract. [PDF]
Wang H +9 more
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Tubular proteinuria due to hereditary endocytic receptor disorder of the proximal tubule: Dent disease and chronic benign proteinuria. [PDF]
Sakakibara N, Nozu K.
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A phosphoinositide switch from PI(4,5)P2 to PI4P triggers endocytosis by inducing dynamin-mediated fission in secretory cells. [PDF]
Guo X +12 more
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Dent disease: clinical practice recommendations. [PDF]
Bökenkamp A +11 more
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Local PI(4,5)P<sub>2</sub> synthesis by septin-associated PIPKIγ isoforms controls centralspindlin association with the midbody during cytokinesis. [PDF]
Russo G +9 more
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Unprecedented coexistence of Dent's disease type 1 and Wilson's disease in a two-year-old Chinese boy: implications for precision medicine. [PDF]
Mao Q +5 more
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Genetic spectrum of congenital cataract with optional ocular and multisystem abnormalities. [PDF]
Zhang H +9 more
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