X-linked muscular atrophy and the androgen receptor
- 31 December 1994
- journal article
- review article
- Published by Elsevier in Trends in Endocrinology & Metabolism
- Vol. 5 (10) , 416-421
- https://doi.org/10.1016/1043-2760(95)92524-m
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Trinucleotide repeats in neurologic diseases: An hypothesis concerning the pathogenesis of Huntington's disease, Kennedy's disease, and spinocerebellar ataxia type ILife Sciences, 1994
- Complete androgen insensitivity due to mutations in the probable -helical segments of the DNA-binding domain in the human androgen receptorHuman Molecular Genetics, 1994
- Human genetic diseases due to codon reiteration: Relationship to an evolutionary mechanismCell, 1993
- Trinucleotide repeat length instability and age of onset in Huntington's diseaseNature Genetics, 1993
- Kennedy's diseaseNeurology, 1993
- Alternative excitotoxic hypothesesNeurology, 1992
- Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groupsGenomics, 1992
- Localization of the gene for X‐linked spinal muscular atrophyNeurology, 1986
- A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failureJournal of the Neurological Sciences, 1983
- X-linked recessive bulbospinal neuronopathy: a report of ten cases.Journal of Neurology, Neurosurgery & Psychiatry, 1982