Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3–p21.2 between D1S2896 and D1S457 but outside ABCA4

Easy calculations of lod scores and genetic risks on small computers.

G.M. Lathrop, J.-M. Lalouel · PubMed · 1984 · 1.5K citations

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Jian Weng, Nathan L. Mata, Sassan M. Azarian et al. · Cell · 1999 · 874 citations · Full text

Protein Function, Signal Transduction, Signaling Pathway +9

Standard for clinical electroretinography

Michael F. Marmor, G. B. Arden, Sven-Erik Nilsson et al. · Documenta Ophthalmologica · 1989 · 810 citations

Electrophysiological Evaluation, Medicine, Patient Safety +7

Avoiding Recomputation in Linkage Analysis

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Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

Andreas Gal, Yun Li, Debra A. Thompson et al. · Nature Genetics · 2000 · 655 citations

Ocular Disease, Retina, Photoreceptor Cell +7