Determining the incidence of familiality in ALS | Neurology Genetics
Discovering the connection between familial and sporadic amyotrophic lateral sclerosis: pathology trumps genetics | Future Neurology
IJMS | Free Full-Text | CRISPR/Cas9-Mediated Gene Correction to Understand ALS
Familial ALS (fALS) gene mutations and clinical features | Download Table
Mutation spectrum of ALS-linked genes in our ALS cohort and Chinese ALS... | Download Scientific Diagram
Mutation and oligomerization of SOD1 can be the reason for Amyotrophic Lateral Sclerosis – ALS Online Database
Frontiers | ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Redefining Sporadic and Familial ALS | InsideALS HCP
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis | Scientific Reports
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public v
Familial ALS (fALS) gene mutations and clinical features | Download Table
Effect of familial clustering in the genetic screening of 235 French ALS families | Journal of Neurology, Neurosurgery & Psychiatry
10 Things to Know About ALS Genetic Testing | ALS News Today
Translating SOD1 Gene Silencing toward the Clinic: A Highly Efficacious, Off-Target-free, and Biomarker-Supported Strategy for fALS: Molecular Therapy - Nucleic Acids
Possible coexisting autoimmunity in a variant case of familial amyotrophic lateral sclerosis associated with antiâ•'<fc&
Genes | Free Full-Text | Investigating the Genetic Profile of the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia (ALS-FTD) Continuum in Patients of Diverse Race, Ethnicity and Ancestry
Frontiers | Novel and Recurrent Mutations in a Cohort of Chinese Patients With Young-Onset Amyotrophic Lateral Sclerosis
Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells - ScienceDirect
Identification of a novel Cys146X mutation of SOD1 in familial amyotrophic lateral sclerosis by whole-exome sequencing | Genetics in Medicine
Frequency of mutated genes in FALS patients. | Download Scientific Diagram
Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China | BMC Medical Genomics | Full Text
Genetic testing and genetic counseling for amyotrophic lateral sclerosis: an update for clinicians | Genetics in Medicine
Neuroprotection by Gene Therapy Targeting Mutant SOD1 in Individual Pools of Motor Neurons Does not Translate Into Therapeutic Benefit in fALS Mice: Molecular Therapy
