Associated Papers
Further delineation of LRSAM1-related Charcot-Marie-Tooth type 2P with parkinsonism.
Ducatel P et al.
European Journal of Medical Genetics, 2025
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P.
Reilich P et al.
Neuromuscular Disorders : Nmd, 2021
LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2.
Peretti A et al.
European Journal of Human Genetics : Ejhg, 2019
Select a paper to view details