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Dive into the research topics of 'Mutations in the glycosyltransferase domain of GLT8D1 are associated with familial amyotrophic lateral sclerosis'. Together they form a unique fingerprint.- Sort by
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Johnathan Cooper-Knock, Tobias Moll, Tennore Ramesh, Lydia Castelli, Alexander Beer, Henry Robins, Ian Fox, Isabell Niedermoser, Philip Van Damme, Matthieu Moisse, Wim Robberecht, Orla Hardiman, Monica P. Panades, Abdelilah Assialioui, Jesus S. Mora, A. Nazli Basak, Karen E. Morrison, Christopher E. Shaw, Ammar Al-Chalabi, John E. Landers
Research output: Contribution to journal › Article › peer-review