Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q

American Journal of Human Genetics

Volumn 74, Issue 4, 2004, Pages 721-730

  Toomes, Carmel ^a,j   Bottomley, Helen M ^a   Jackson, Richard M ^a   Towns, Katherine V ^a   Scott, Sheila ^a   Mackey, David A ^b   Craig, Jamie E ^b,c   Jiang, Li ^d   Yang, Zhenglin ^d   Trembath, Richard ^e   Woodruff, Geoffrey ^e   Gregory Evans, Cheryl Y ^f   Gregory Evans, Kevin ^f   Parker, Michael J ^g   Black, Graeme C M ^h,i   Downey, Louise M ^a   Zhang, Kang ^d   Inglehearn, Chris F ^a  

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b ROYAL VICTORIAN EYE AND EAR HOSPITAL   (Australia)

^c FLINDERS MEDICAL CENTRE   (Australia)

^d UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^e UNIVERSITY OF LEICESTER   (United Kingdom)

^f IMPERIAL COLLEGE LONDON   (United Kingdom)

^g SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

^h UNIVERSITY OF MANCHESTER   (United Kingdom)

ⁱ ST MARY S HOSPITAL   (United Kingdom)

^j ST JAMES S UNIVERSITY HOSPITAL   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

FRIZZLED 4 PROTEIN; FRIZZLED PROTEIN; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN 5; UNCLASSIFIED DRUG; WNT PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLINDNESS; CHROMOSOME 11Q; EVR1 GENE; FAMILIAL DISEASE; FAMILIAL EXUDATIVE VITREORETINOPATHY; GENE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; HUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RETINA BLOOD VESSEL; SIGNAL TRANSDUCTION; VASCULARIZATION; VITREORETINOPATHY;

EID: 12144288372     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/383202     Document Type: Article

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