Concepedia

Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness

Christina Zeitz, Barbara Kloeckener‐Gruissem, U. Förster, Susanne Kohl, I Magyar, Bernd Wissinger, Gábor Mátyás, François‐Xavier Borruat, Daniel F. Schorderet, Eberhart Zrenner,

The American Journal of Human Genetics · 2006 · 181 citations · 38 references

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38

A simple salting out procedure for extracting DNA from human nucleated cells

S.A. Miller, Dale D. Dykes, Herbert F. Polesky · Nucleic Acids Research · 1988 · 20.6K citations · Full text

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Improved Splice Site Detection in Genie

Martin G. Reese, Frank H. Eeckman, David Kulp et al. · Journal of Computational Biology · 1997 · 1.6K citations

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Improved splice site detection in Genie

Martin G. Reese, Frank H. Eeckman, David Kulp et al. · 1997 · 1.5K citations

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Standard for clinical electroretinography

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

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Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Bech-Hansen Nt, Ben F. Koop, M. B. Mets et al. · Nature Genetics · 1998 · 518 citations

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