Mutations in the SPTLC1 gene are a cause of amyotrophic lateral sclerosis that may be amenable to serine supplementation
Authors
Janel Johnson,
Ruth ChiaRavindran Kumaran,
Nada Alahmady,
Danny Miller,
Yevgeniya Abramzon,
Faraz Faghri,
Alan Renton,
Simon Topp,
Hannah Pliner,
J. Gibbs,
Jinhui Ding,
Nathan Smith,
Natalie Landeck,
Michael Nalls,
Mark Cookson,
Olga Pletnikova,
Juan Troncoso,
Sonja Scholz,
Marya Sabir,
Sarah Ahmed,
Clifton Dalgard,
Claire Troakes,
Ashley Jones,
Aleksey Shatunov,
Alfredo Iacoangeli,
Ahmad Khleifat,
Nicola Ticozzi,
Vincenzo Silani,
Cinzia Gellera,
Ian Blair,
Carol Dobson-Stone,
John Kwok,
Bryce England,
Emily Bonkowski,
The Consortium,
The Center,
Pentti Tienari,
David Stone,
Karen Morrison,
Pamela Shaw,
Ammar Al-Chalabi,
Robert Brown,
Maura Brunetti,
Andrea Calvo,
Gabriele Mora,
Marc Gotkine,
Fawn Leigh,
Ian Glass,
Christopher Shaw,
John Landers,
Adriano Chiò,
Thomas Crawford,
Bradley Smith,
Bryan Traynor,
Jamlik-Omari Johnson,
Rong Li,
R. Kumaran,
Mike Nalls,
Olga Pletniková,
M. Sabir,
I‐Jing Chang,
Bret Smith,
Carol Dobson‐Stone,
B England,
Maura Pugliatti,
Haytham AlSaif,
Marc Guillaume,
I. Chang,
Steve Perlman +68 authors
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Ammar Al‐Chalabi Tip Tip