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1. MYO7A mutation screening in Usher syndrome type I patients from diverse origins.

Author

Jaijo T, Aller E, Beneyto M, Najera C, Graziano C, Turchetti D, Seri M, Ayuso C, Baiget M, Moreno F, Morera C, Perez-Garrigues H, and Millan JM

Subjects
Amino Acid Sequence, Codon, Nonsense, Czech Republic ethnology, DNA Mutational Analysis, Female, Humans, Italy ethnology, Male, Molecular Sequence Data, Morocco ethnology, Mutagenesis, Insertional, Mutation, Missense, Myosin VIIa, Pedigree, Point Mutation, Polymorphism, Single-Stranded Conformational, RNA Splice Sites genetics, Sequence Alignment, Sequence Deletion, Sequence Homology, Amino Acid, Spain ethnology, Tandem Repeat Sequences, Turkey ethnology, Usher Syndromes ethnology, Dyneins genetics, Mutation, Myosins genetics, Usher Syndromes genetics
Published
2007
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