A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration

Human Molecular Genetics

Volumn 9, Issue 1, 2000, Pages 27-34

  Maw, Marion A ^a   Corbeil, Denis ^b,c   Koch, Julia ^b,c   Hellwig, Andrea ^b,c   Wilson Wheeler, Jane C ^a   Bridges, Robyn J ^a   Kumaramanickavel, Govindasamy ^d   John, Sheila ^d   Nancarrow, Derek ^e   Röper, Katja ^b,c   Weigmann, Anja ^b,c   Huttner, Wieland B ^b,c   Denton, Michael J ^a  

^a UNIVERSITY OF OTAGO   (New Zealand)

^b UNIVERSITY OF HEIDELBERG   (Germany)

^c MAX PLANCK INSTITUTE OF MOLECULAR CELL BIOLOGY AND GENETICS   (Germany)

^d MEDICAL RESEARCH FOUNDATION   (India)

^e WOLSTON PARK HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; PROMININ; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CELL LINE; CELL SURFACE; CHO CELL; CLINICAL ARTICLE; CONTROLLED STUDY; DELETION MUTANT; EMBRYO; EPITHELIUM CELL; FRAMESHIFT MUTATION; GENETIC ANALYSIS; HUMAN; HUMAN CELL; IMMUNOCYTOCHEMISTRY; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOTORECEPTOR; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETINA DEGENERATION; RETINOBLASTOMA;

ANIMALIA; MURINAE; VERTEBRATA;

EID: 0034101383     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.1.27     Document Type: Article

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