Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34
Article Abstract:
An autosomal dominant form of juvenile amyotrophic lateral sclerosis (ALS) has been linked to a gene, ALS4, on chromosome 9q34. A gene on that chromosome is implicated as being important for motor-neuron function. Genetic mapping was carried out on an 11-generation pedigree that had the autosomal dominant, juvenile-onset motor-systems disease. The highest LOD score was found with D9S1847. Results extend the degree of heterogeneity within familial ALS syndromes.
Publication Name: American Journal of Human Genetics
Subject: Biological sciences
ISSN: 0002-9297
Year: 1998
User Contributions:
Comment about this article or add new information about this topic:
The gene for cherubism maps to chromosome 4p16
Article Abstract:
The gene for cherubism, an autosomal dominant disorder perhaps related to tooth development and eruption and resulting in altered facial appearance and large amounts of fibrous tissue in the jaws, has been mapped to chromosome 4p16. A genomewide search has been carried out in a 3-generation family. Three other affected families were genotyped and mapped to the locus, which is across an interval of about 22 cM.
Publication Name: American Journal of Human Genetics
Subject: Biological sciences
ISSN: 0002-9297
Year: 1999
User Contributions:
Comment about this article or add new information about this topic:
- Abstracts: Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22. Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
- Abstracts: Mitochrondrial dysfunction in idiopathic Parkinson disease. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q
- Abstracts: Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28. Genetic linkage of hereditary gingival fibromatosis to chromosome 2p21
- Abstracts: Mapping of primary congenital lymphedema to the 5q35.3 region. A new locus for autosomal dominant Stargardt-like disease maps to chromosome 4