Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment. [electronic resource]
- Human mutation Dec 2001
- 548 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1098-1004
10.1002/humu.1238 doi
Alleles Carrier Proteins--genetics DNA--chemistry DNA Mutational Analysis Family Health Genotype Goiter--complications Hearing Disorders--genetics Hearing Loss, Sensorineural--complications Humans Italy Membrane Transport Proteins Mutation Phenotype Spain Sulfate Transporters Syndrome