Hereditary spastic paraplegia Scholarly journal
Genetic spastic paraparesis (HSP) or the Strümpell-Lorrain disorder is the name given to a heterogeneous gathering of acquired issue in which the principle clinical element is dynamic lower appendage spasticity. Before the coming of atomic hereditary examinations into these clutters, a few characterizations had been proposed, in view of the method of legacy, the time of beginning of manifestations, and the nearness or in any case of extra clinical highlights. Families with autosomal predominant, autosomal latent
, furthermore, X-connected legacy have been depicted
Review Article: Journal of Genetics and Genomes
Review Article: Journal of Genetics and Genomes
Short Communication: Journal of Genetics and Genomes
Short Communication: Journal of Genetics and Genomes
Research Article: Journal of Genetics and Genomes
Research Article: Journal of Genetics and Genomes
Editorial: Journal of Genetics and Genomes
Editorial: Journal of Genetics and Genomes
Editorial: Journal of Genetics and Genomes
Editorial: Journal of Genetics and Genomes
Scientific Tracks Abstracts: Molecular and Genetic Medicine
Scientific Tracks Abstracts: Molecular and Genetic Medicine
Scientific Tracks Abstracts: Molecular and Genetic Medicine
Scientific Tracks Abstracts: Molecular and Genetic Medicine
Accepted Abstracts: Molecular and Genetic Medicine
Accepted Abstracts: Molecular and Genetic Medicine
Scientific Tracks Abstracts: Metabolomics:Open Access
Scientific Tracks Abstracts: Metabolomics:Open Access
Posters: Metabolomics:Open Access
Posters: Metabolomics:Open Access
Journal of Genetics and Genomes received 65 citations as per Google Scholar report