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Gene Information
Gene symbol: BSND
Gene name: Bartter syndrome, infantile, with sensorineural deafness (Barttin)
HGNC ID: 16512
Synonyms: BART
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | KCNJ1 | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 18446382 | Thus, Bartter syndrome, an autosomal disease, is caused by mutations of the bumetanide-sensitive Na-K-Cl (NKCC2) co-transporter, the renal outer-medullary potassium (ROMK) channel, the voltage-gated chloride channel, CLC-Kb, the CLC-Kb beta subunit, barttin, or the calcium-sensing receptor (CaSR). |