Different origins of mutations at the Machado-Joseph locus (MJD1)
Open Access
- 1 May 1996
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 33 (5) , 439
- https://doi.org/10.1136/jmg.33.5.439
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
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- Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado‐Joseph diseaseAnnals of Neurology, 1995
- Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patientsHuman Molecular Genetics, 1995
- Molecular features of the CAG repeats and clinical manifestation of Machado--Joseph diseaseHuman Molecular Genetics, 1995
- The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.1995
- CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1Nature Genetics, 1994
- A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.1994
- The gene for Machado–Joseph disease maps to human chromosome 14qNature Genetics, 1993
- Machado‐Joseph disease: An autosomal dominant motor system degenerationMovement Disorders, 1992
- [Clinical, genetic and pathological aspects of Machado-Joseph disease].1981