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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

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Year: 2005
Type: article
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddi044
Authors: Nùria Fonknechten, Delphine Mavel, Paula Byrne, Claire-Sophie Davoine, Corinne Cruaud, Dominikus Bönsch, Delphine Samson, Paula Coutinho, Michael Hutchinson, Paul McMonagle, Jean-Marc Burgunder, Antonio Tartaglione, Olivier Heinzlef, Imed Feki, Thomas Deufel, Nollaig Parfrey, Alexis Brice, Bertrand Fontaine, Jean-François Prud'homme, Jean Weissenbach, Alexandra Dürr, Jamilé Hazan
Language: English

Topic: Hereditary Neurological Disorders
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W4243391952
FWCI:
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Related to: 10
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