Genomic structure and identification of novel mutations in Usherin, the gene responsible for usher syndrome type IIa

Biochemistry, Genetics and Molecular Biology

• Allele 100%
• Exon 100%
• Laminin 100%
• Genomic Structure 100%
• Polymerase Chain Reaction 66%
• USH2A 66%
• Epidermal Growth Factor 33%
• Autosomal Recessive Disorder 33%
• Fibronectin Type III Domain 33%
• Human Chromosome 33%
• Retinitis pigmentosa 33%
• Molecular Weight 33%
• Intron 33%
• Missense Mutation 33%
• Cell Adhesion Molecule 33%
• Heteroduplex Analysis 33%
• Homozygote 33%
• Proband 33%
• Basal Lamina 33%

Keyphrases

• Mutation Search 20%
• Network Assembly 20%