Cells | Free Full-Text | Pathogenic Genome Signatures That Damage Motor Neurons in Amyotrophic Lateral Sclerosis
Mutation and oligomerization of SOD1 can be the reason for Amyotrophic Lateral Sclerosis – ALS Online Database
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public v
List of fALS genes and loci | Download Table
Determining the incidence of familiality in ALS | Neurology Genetics
Genetic ALS: An Overview of Common Mutations| InsideALS HCP
Theme 2 Genetics and genomics
Possible coexisting autoimmunity in a variant case of familial amyotrophic lateral sclerosis associated with antiâ•'<fc&
Neuroprotection by Gene Therapy Targeting Mutant SOD1 in Individual Pools of Motor Neurons Does not Translate Into Therapeutic Benefit in fALS Mice: Molecular Therapy
Frontiers | ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Genetic testing practices for suspected familial cases of ALS (fALS).... | Download Scientific Diagram
Translating SOD1 Gene Silencing toward the Clinic: A Highly Efficacious, Off-Target-free, and Biomarker-Supported Strategy for fALS: Molecular Therapy - Nucleic Acids
Frequency of mutated genes in FALS patients. | Download Scientific Diagram
Discovering the connection between familial and sporadic amyotrophic lateral sclerosis: pathology trumps genetics | Future Neurology
Gene frequencies in ALS. Notes: Each gene is plotted against the year... | Download Scientific Diagram
Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis | Journal of Neurology, Neurosurgery & Psychiatry
Rare Disease Series #24: Amyotrophic Lateral Sclerosis
Frontiers | The Neglected Genes of ALS: Cytoskeletal Dynamics Impact Synaptic Degeneration in ALS
Familial ALS (fALS) gene mutations and clinical features | Download Table
Redefining Sporadic and Familial ALS | InsideALS HCP
Familial ALS (fALS) gene mutations and clinical features | Download Table
Molecular mechanisms of amyotrophic lateral sclerosis (ALS) and related neurodegenerative disorders - TS Lab
Genetic testing and genetic counseling for amyotrophic lateral sclerosis: an update for clinicians | Genetics in Medicine
Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China | BMC Medical Genomics | Full Text
Redefining Sporadic and Familial ALS | InsideALS HCP
The genetics of amyotrophic lateral sclerosis: current insights | DNND
