Work

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nat Gen 2000;24:79–83.

Year: 2000

Type: article

Study design: Observational Study

Source: American Journal of Ophthalmology

DOI: 10.1016/s0002-9394(00)00517-1

Authors: M.M Sohoki, S.J Browne, L.S Sullivan, S Blackshaw, C.L Cepko, A.M Payne, S.S Bhattacharya, S Khaliq, S.Q Mehdi, D.G Birch, W.R Harrison, F.F.B Elder, J.R Heckenlively, S.P Daiger

Institutions: The University of Texas Health Science Center at Houston, Howard Hughes Medical Institute, Harvard University, University College London, Retina Foundation of the Southwest, University of California, Los Angeles

Language: English

Topic: Retinal Development and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: George Gund Foundation, Wellcome Trust, National Institutes of Health, Medical Research Council, National Eye Institute

Awards: DNA Linkage Studies of Degenerative Retinal Diseases, G8696398973

OpenAlex ID: W2053828264

FWCI:

Cites: 11

Cited by: 10

Related to: 10