Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. [electronic resource]
Producer: 20090508Description: 474-82 p. digitalISSN:- 1476-5438
- Amino Acid Sequence
- Base Sequence
- Consanguinity
- Cyclic Nucleotide Phosphodiesterases, Type 6 -- genetics
- Family
- Hearing Loss -- congenital
- Humans
- Molecular Sequence Data
- Mutation
- Pedigree
- Phenotype
- Receptors, G-Protein-Coupled -- genetics
- Retinal Degeneration -- genetics
- Retinitis Pigmentosa -- genetics
- Tunisia
- Usher Syndromes -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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