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Results 1 - 5 of 5 for Leber congenital amaurosis 10
  1. GUCY2D gene 
    ... GUCY2D mutation causing cone-rod dystrophy and not Leber's congenital amaurosis. Eur J Hum Genet. 2010 Oct;18(10):1121-6. doi: 10.1038/ejhg.2010.81. ...
    https://medlineplus.gov/genetics/gene/gucy2d - Genetics
  2. CRB1 gene 
    ... Stone EM. Mutations in the CRB1 gene cause Leber congenital amaurosis. Arch Ophthalmol. 2001 Mar;119(3):415-20. doi: 10.1001/archopht.119.3.415. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/crb1 - Genetics
  3. CEP290 gene 
    ... CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis. Am J Hum Genet. 2006 Sep;79(3):556-61. doi: 10.1086/507318. Epub 2006 Jul 11. Citation on ...
    https://medlineplus.gov/genetics/gene/cep290 - Genetics
  4. RPE65 gene 
    ... in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. Proc Natl Acad Sci U S A. 1998 Mar 17;95(6):3088-93. doi: 10.1073/pnas.95.6.3088. Citation on PubMed ...
    https://medlineplus.gov/genetics/gene/rpe65 - Genetics
  5. CRX gene 
    ... This Health Condition MedlinePlus Genetics provides information about Leber congenital amaurosis More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/crx - Genetics