Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
Hmani-Aifa, Mounira
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. [electronic resource] - European journal of human genetics : EJHG Apr 2009 - 474-82 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1476-5438
10.1038/ejhg.2008.167 doi
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
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. [electronic resource] - European journal of human genetics : EJHG Apr 2009 - 474-82 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1476-5438
10.1038/ejhg.2008.167 doi
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