PDS

abbr.

potential differences 电位差，电势差；

A mutation in PDS causes non-syndromic recessive deafness
The high energy instrument PDS on-board the BeppoSAX X--ray astronomy satellite
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome
Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations.
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations
Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged v...
Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by th...
Everett, L.A. et al. Pendred syndrome is caused by mutations in a putative sulphate transporter (PDS). Nature Genet. 17, 411-422