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Journal Article
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, pp. e0177955 - e0177955
Spinocerebellar ataxia type 10 (SCA10) is an autosomal-dominant cerebellar ataxia that is variably accompanied by epilepsy and other neurological disorders. It... 
ATTCT REPEAT EXPANSION | SCA10 | POPULATION | RNA TOXICITY | MULTIDISCIPLINARY SCIENCES | DISEASE | PHENOTYPE | BRAZILIAN FAMILIES | MODEL | HEXANUCLEOTIDE REPEAT | FREQUENCY-ANALYSIS | Cerebellum | Brain | Divergence | RNA | Disease | Radiation | Cognitive ability | Nervous system | Leukocytes | Chains (polymeric) | Epidemiology | Fragmentation | Genotype & phenotype | Ataxin | Coding | Neurodegeneration | Ataxia | Biocompatibility | Genetics | Expansion | Deoxyribonucleic acid--DNA | Cellulose esters | Neurodegenerative diseases | Cerebellar ataxia | Japan | Committees | Hereditary diseases | Diseases | Amplification | Neurological diseases | Polymerase chain reaction | Neurology | Ribonucleic acids | Frequency analysis | Mice | Mutation | Continents | Frontotemporal dementia | Dementia | Health care | Haplotypes | Health sciences | Neurosciences | Arches | Toxicity | Epilepsy | Genes | Population studies | Genomes | Biology | Mental retardation | Atrophy | Biomedical materials | China | Cellulose nitrate | Dementia disorders | Population | Degeneration | Islands | University graduates | Cognitive impairment | Geographical distribution | Nucleotide sequence | Health | Amyotrophic lateral sclerosis | Medicine | Corneal dystrophy | Asia | DNA | Dystrophy | Genetic testing | Gene mapping | Psychiatry | Colonization | DNA Repeat Expansion - genetics | Humans | Middle Aged | Male | Microsatellite Repeats - genetics | Phenotype | Ataxin-10 - genetics | Pedigree | Polymorphism, Single Nucleotide - genetics | Female | Aged | Spinocerebellar Ataxias - genetics | Care and treatment | Gene mutations | Spinocerebellar ataxia | Patient outcomes | Research | Risk factors | Ribonucleic acid--RNA | Index Medicus | Deoxyribonucleic acid | Ribonucleic acid
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 08/2003, Volume 44, Issue 8, pp. 3310 - 3316
Journal Article
Journal Article
2014, 1st Edition., ISBN 9783540694649, 477
This lavishly illustrated atlas provides indispensable information to clinicians, geneticists and visual scientists working with inherited retinal diseases. It... 
Retinal degeneration | Other branches of medicine | Retina | Genetic aspects | Diseases | Atlases | Human Genetics | Pathology | Ophthalmology | Medicine & Public Health
eBook
Journal Article