LCA5 gene

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^[1]

Introduction

6q14.1

Pathology

defect in LCA5 gene associated with Leber congenital amaurosis

More general terms

unclassified gene

References

↑ den Hollander AI et al, Mutations encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. Nat Genet 2007, 39:889 PMID: https://www.ncbi.nlm.nih.gov/pubmed/17546029

Database

Entrez gene: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=167691

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