DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4) - Chen, Ying-Zhang; Bennett, Craig L.; Huynh, Huy M.; Blair, Ian P.; Puls, Imke; Irobi, Joy; Dierick, Ines; Abel, Annette; Kennerson, Marina L.; Rabin, Bruce A.; Nicholson, Garth A.; Auer-Grumbach, Michaela; et al. (American journal of human genetics, 2004)
Keywords: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Amino Acid Sequence; Amyotrophic Lateral Sclerosis - genetics; Animals; Autopsy; Base Sequence; Biological and medical sciences; Child; Chromosome Mapping; Chromosomes, Human, Pair 9 - genetics; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; DNA - genetics; DNA Helicases; Female; Genes, Dominant; Genetic Linkage; Humans; Hybrid Cells; Male; Medical sciences; Mice; Molecular Sequence Data; Multifunctional Enzymes; Mutation, Missense - genetics; Neurology; Pedigree; RNA Helicases - genetics; Sequence Homology, Amino Acid; Nervous system diseases; Gene; RNA; DNA; Central nervous system disease; Amyotrophic lateral sclerosis; Degenerative disease; Mutation; Spinal cord disease