Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutations. [electronic resource]
Producer: 20040713Description: 1-9 p. digitalISSN:- 1552-4825
- Biological Transport
- Carrier Proteins -- genetics
- Chromatography, High Pressure Liquid
- DNA Mutational Analysis
- DNA Primers
- Diagnosis, Differential
- Genetic Testing
- Goiter -- diagnosis
- Hearing Loss, Sensorineural -- diagnosis
- Humans
- Membrane Transport Proteins
- Polymorphism, Genetic
- Polymorphism, Single-Stranded Conformational
- Sensitivity and Specificity
- Sequence Analysis, DNA
- Sulfate Transporters
- Sulfates
- Syndrome
No physical items for this record
Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.