A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome. [electronic resource]
Producer: 20050401Description: 306-8 p. digitalISSN:- 0003-9942
- Adult
- DNA Mutational Analysis -- methods
- Deafness -- genetics
- Family Health
- Female
- Genetic Diseases, X-Linked -- genetics
- Humans
- Introns -- genetics
- Male
- Membrane Transport Proteins -- genetics
- Mitochondrial Precursor Protein Import Complex Proteins
- Mutation -- genetics
- Pedigree
- RNA, Messenger -- biosynthesis
- Reverse Transcriptase Polymerase Chain Reaction -- methods
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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