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Mutations in LRP5 or FZD4 Underlie the Common Familial Ex... | ResearchHub
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Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q
0
Authors
Carmel Toomes
17 more
Carmel Toomes
•
H.M. Bottomley
15 more
•
Chris Inglehearn
Published
March 17, 2004
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Journal
The American Journal of Human Genetics
Topics
Biology
Neurology
Molecular Biology
Phenotype
Wnt Signaling Pathway
Show all topics
DOI
10.1086/383202
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publisher-specific-oa
Supporters
Support the authors with ResearchCoin
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Journal
The American Journal of Human Genetics
Topics
Biology
Neurology
Molecular Biology
Phenotype
Wnt Signaling Pathway
Show all topics
DOI
10.1086/383202
License
publisher-specific-oa
