This table has been prepared by Dr Gisèle Bonne * - PhD and by Pr. François Rivier ** - MD, PhD
This website is developed and maintained by Dalil Hamroun** - PhD
* Sorbonne Université-Inserm, Centre of Research in Myology , Paris, France.
** Chu de Montpellier, Montpellier. France.
GT_NMD 2024 (updated 17/01/2024)
Gene symbol and protein | Gene Location | All allelic disease phenotypes - locus/disease symbols |
ATL1 Atlastin GTPase 1       | 14q22.1 | * Spastic paraplegia 3, autosomal dominant (Strumpell disease) - SP3A (14.118, 15.1)* Neuropathy, hereditary sensory, type ID - HSN1D (14.118, 15.1) |