Elsevier

Pediatric Neurology

Volume 134, September 2022, Page 71
Pediatric Neurology

Correspondence
Infantile-Onset Complex Hereditary Spastic Paraplegia Due to a Novel Mutation in SPAST Gene

https://doi.org/10.1016/j.pediatrneurol.2022.06.020Get rights and content

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Disclosures: A.V. has worked in advisory or consulting capacity with PTC Therapeutics, Novartis, Sarepta, Biogen, ScholarRock, Fibrogen, and NS Pharma. A.V. has received grant or research support from Sarepta, Fibrogen, Novartis, Genentech, AMGEN, Impax Labs, Teva, Ely Lilly, AMO Pharma, Pfizer, and Octapharma. Other authors report no disclosures.

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