Concepedia

U1 snRNA mis-binding: a new cause of CMT1B

Hervé Crehalet, Philippe Latour, Véronique Bonnet, Shahram Attarian, Pierre Labauge, Nathalie Bonello‐Palot, Rafaëlle Bernard, Gilles Millat, Robert Rousson, Dominique Bozon

Neurogenetics · 2009 · 18 citations · 23 references

DOI

Concepts

References

23

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

François-Olivier Desmet, Dalil Hamroun, Marine Lalande et al. · Nucleic Acids Research · 2009 · 2.5K 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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Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons

Karl-Peter Giese, Rudolf Martini, Greg Lemke et al. · Cell · 1992 · 495 citations

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Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations

Ken Inoue, Mehrdad Khajavi, Tomoko Ohyama et al. · Nature Genetics · 2004 · 421 citations

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