López-Bigas, N

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