MeSH Browser

MeSH Supplementary: BSND protein, human
Unique ID: C440005
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C440005
Entry Term(s): Bartter syndrome, infantile, with sensorineural deafness protein, human; DFNB73 protein, human; barttin protein, human
Registry Numbers: 0
Previous Indexing: *PROTEINS (2001-2008)
Heading Mapped to: *Chloride Channels
Frequency: 51
Note: a chloride channel beta-subunit; mutations leads to Bartter syndrome with sensorineural deafness and kidney failure; RefSeq NM_057176
Source: Nat Genet 2001 Nov;29(3):310-4
Indexing Information: Protein Subunits
Date of Entry: 2001/12/01
Revision Date: 2009/09/22

BSND protein, human MeSH Supplementary Concept Data 2025