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UnknownMuscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
Not available
S-EPMC3213389 | biostudies-literature
UnknownMutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement.
Not available
S-EPMC1698561 | biostudies-literature
UnknownDefects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.
Not available
S-EPMC8259640 | biostudies-literature
UnknownRefining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis.
Not available
S-EPMC9459005 | biostudies-literature
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