Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease

Investigative Ophthalmology and Visual Science

Volumn 38, Issue 3, 1997, Pages 704-709

  Parminder, Amy H ^a   Murakami, Akira ^b   Inana, George ^b   Berson, Eliot L ^a   Dryja, Thaddeus P ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^b UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Bardet Biedl syndrome; Leber congenital amaurosis; recoverin; retinitis pigmentosa; Usher syndrome

Indexed keywords

RECOVERIN;

ARTICLE; BARDET BIEDL SYNDROME; CONTROLLED STUDY; GENE MUTATION; GENE SEQUENCE; HUMAN; HUMAN CELL; HUMAN TISSUE; LEBER CONGENITAL AMAUROSIS; MAJOR CLINICAL STUDY; PHENOTYPE; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; SEQUENCE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; USHER SYNDROME;

CALCIUM-BINDING PROTEINS; DEAFNESS; DNA; DNA PRIMERS; EXONS; EYE PROTEINS; FEMALE; HIPPOCALCIN; HUMANS; LAURENCE-MOON SYNDROME; LIPOPROTEINS; MALE; NERVE TISSUE PROTEINS; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RECOVERIN; RETINITIS PIGMENTOSA;

EID: 0030989004     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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