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Nature genetics, ISSN 1061-4036, 1999, Volume 23, Issue 2, pp. 217 - 221
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases that afflicts approximately 1.5 million people worldwide.... 
PROTEIN | GENE | EPITHELIAL-CELL LINE | LAMININ | SEQUENCE | GENETICS & HEREDITY | RECEPTOR | EPIDERMAL GROWTH-FACTOR | PROTEOGLYCAN | DOMAINS | EXPRESSION | CRB1 protein | amino acid sequence prediction | Retina | nucleotide sequence | RET3C11 gene | Laminin | chromosome 1 | retinitis pigmentosa | Lectins | Photoreceptors | cDNA | man | epidermal growth factor | crumbs protein | Humans | Molecular Sequence Data | Family Health | Male | Polymorphism, Single-Stranded Conformational | Tissue Distribution | crumbs protein, Drosophila | Chromosomes, Human, Pair 1 | Retinitis Pigmentosa | DNA Mutational Analysis | Gene Expression Regulation, Developmental | Base Sequence | Female | Amino Acid Sequence | Cell Line | Drosophila Proteins | Chromosome Mapping | Sequence Analysis, DNA | Index Medicus | Membrane Proteins | Homozygote | Point Mutation | Blotting, Northern | Animals | Pedigree | Mutagenesis, Insertional | Mutation | Alu Elements | Drosophila melanogaster | Eye Proteins | RNA, Messenger | Amino Acid Substitution | DNA, Complementary | DNA, Complementary - genetics | RNA, Messenger - metabolism | Drosophila melanogaster - genetics | Eye Proteins - genetics | Chromosomes, Human, Pair 1 - genetics | Alu Elements - genetics | Membrane Proteins - genetics | RNA, Messenger - genetics | Retinitis Pigmentosa - genetics | DNA, Complementary - chemistry | Retinitis Pigmentosa - pathology
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 1999, Volume 64, Issue 4, pp. 1024 - 1035
Journal Article
Human Mutation, ISSN 1059-7794, 2004, Volume 24, Issue 2, pp. 185 - 185
Usher syndrome type II (USH2) is characterised by moderate to severe high-frequency hearing impairment, progressive visual loss due to retinitis pigmentosa and... 
usherin | Usher syndrome | retinitis pigmentosa | hearing impairment | mutation screening | genotype phenotype | USH2A | Dutch | Haplotypes - genetics | Extracellular Matrix Proteins - genetics | Genetic Markers - genetics | Humans | Netherlands - epidemiology | Polymorphism, Single Nucleotide - genetics | DNA Mutational Analysis - methods | Index Medicus
Journal Article
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 08/1999, Volume 237, Issue 8, pp. 629 - 635
Journal Article
Journal Article
Annals of Otology, Rhinology and Laryngology, ISSN 0003-4894, 2003, Volume 112, Issue 6, pp. 525 - 530
Journal Article