Infantile-Onset Ascending Hereditary Spastic Paralysis Is Associated with Mutations in the Alsin Gene
- 1 September 2002
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 71 (3), 518-527
- https://doi.org/10.1086/342359
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60American Journal of Human Genetics, 2002
- A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18qAmerican Journal of Human Genetics, 2002
- Hereditary spastic paraparesis: a review of new developmentsJournal of Neurology, Neurosurgery & Psychiatry, 2000
- A New Locus for Autosomal Recessive Spastic Paraplegia Associated with Mental Retardation and Distal Motor Neuropathy, SPG14, Maps to Chromosome 3q27-q28American Journal of Human Genetics, 2000
- Genetic Mapping to 10q23.3-q24.2, in a Large Italian Pedigree, of a New Syndrome Showing Bilateral Cataracts, Gastroesophageal Reflux, and Spastic Paraparesis with AmyotrophyAmerican Journal of Human Genetics, 1999
- A Yeast Artificial Chromosome-Based Physical Map of the Juvenile Amyotrophic Lateral Sclerosis (ALS2) Critical Region on Human Chromosome 2q33–q34Genomics, 1999
- Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34American Journal of Human Genetics, 1998
- X–linked spastic paraplegia and Pelizaeus–Merzbacher disease are allelic disorders at the proteolipid protein locusNature Genetics, 1994
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993
- Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.Journal of Neurology, Neurosurgery & Psychiatry, 1981