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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease distal renal tubular acidosis
Comorbidity C0155550|neural deafness
Sentences 1
PubMedID- 25517796 Mutations in exons 3 and 7 resulting in truncated expression of human atp6v1b1 gene showing structural variations contributing to poor substrate binding-causative reason for distal renal tubular acidosis with sensorineural deafness.

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