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. 2022 Jan 5;11(1):77. doi: 10.3390/biology11010077
MND motor neuron disease
HSP Hereditary Spastic Paraplegia
IAHSP Infantile-onset ascending hereditary spastic paralysis
JPLS Juvenil Primary Lateral Sclerosis
ALS Amyotrophic Lateral Sclerosis
JALS Juvenil Amyotrophic Lateral Sclerosis
ALS2 Amyotrophic Lateral Sclerosis type 2
GEF guanine exchange factor
GTPases guanosine triphosphatases
RCC1 Regulator of Chromosome Condensation 1
RLD RCC1-like domain
DH central B cell lymphoma homology
PH pleckstrin homology
VPS9 vacuolar protein-sorting 9
MORN membrane occupation and recognition nexus
IDR intrinsically disordered region
Ran Ras-related nuclear
LMN lower motor neurons
GRIP1 glutamate receptor-interacting protein 1
AMPA a-amino-3-hydroxy-5-methylisoxazole-4-propio-nate
ALS2(−;−): ALS2 knockout homozygous
SOD1 Cu/Zn-superoxide dismutase
IGF1 insulin-like growth factor
EEA1 early endosome-associated protein
PAK1 p21-activated kinase