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UnknownLocalization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34.
Not available
S-EPMC1288376 | biostudies-literature
UnknownKCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function.
Not available
S-EPMC2922599 | biostudies-literature
UnknownPhase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial.
Not available
S-EPMC8425611 | biostudies-literature
UnknownUrinary tract effects of HPSE2 mutations.
Not available
S-EPMC4378092 | biostudies-literature
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