A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34
- 1 February 2000
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 66 (2), 702-707
- https://doi.org/10.1086/302776
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A New Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Mapping to Chromosome 12q13, and Evidence for Further Genetic HeterogeneityAmerican Journal of Human Genetics, 1999
- Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8qAmerican Journal of Human Genetics, 1999
- A Gene for Autosomal Recessive Symmetrical Spastic Cerebral Palsy Maps to Chromosome 2q24-25American Journal of Human Genetics, 1999
- Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2Brain, 1996
- Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaNeuromuscular Disorders, 1995
- X–linked spastic paraplegia and Pelizaeus–Merzbacher disease are allelic disorders at the proteolipid protein locusNature Genetics, 1994
- Hereditary "pure" spastic paraplegia: a study of nine families.Journal of Neurology, Neurosurgery & Psychiatry, 1993
- The Skeletal Muscle Chloride Channel in Dominant and Recessive Human MyotoniaScience, 1992
- Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.Journal of Neurology, Neurosurgery & Psychiatry, 1981
- Strumpell's familial spastic paraplegia: genetics and neuropathologyJournal of Neurology, Neurosurgery & Psychiatry, 1974