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Autosomal recessive ataxias are much less well studied than autosomal dominant ataxias and there are no clearly defined systems to classify them. Autosomal recessive ataxias, which are characterized by neuronal and multisystemic...

Zebrafish hereditary recessive ataxias neurodegenerative disorders genetic edition

Hereditary dominant ataxias are a heterogeneous group of neurodegenerative conditions causing cerebellar dysfunction and characterized by progressive motor incoordination. Despite many efforts put into the study of these...

X-fragile expanded repeats genetic edition hereditary dominant ataxias neurodegenerative disorders Spinocerebellar Ataxias Zebrafish Animals Arthrogryposis ataxia Disease Models Animal Humans Phenotype Spinocerebellar Degenerations Zebrafish

Autosomal recessive ataxias are much less well studied than autosomal dominant ataxias and there are no clearly defined systems to classify them. Autosomal recessive ataxias, which are characterized by neuronal and multisystemic...

genetic edition hereditary recessive ataxias neurodegenerative disorders Zebrafish Animals ataxia Disease Models Animal Genes Recessive Mutation Zebrafish Zebrafish Proteins

Hereditary dominant ataxias are a heterogeneous group of neurodegenerative conditions causing cerebellar dysfunction and characterized by progressive motor incoordination. Despite many efforts put into the study of these...

Zebrafish hereditary dominant ataxias Spinocerebellar Ataxias expanded repeats X-fragile neurodegenerative disorders genetic edition

NOP56 belongs to a C/D box small nucleolar ribonucleoprotein complex that is in charge of cleavage and modification of precursor ribosomal RNAs and assembly of the 60S ribosomal subunit. An intronic expansion in NOP56 gene...

Animal models genetic edition neurodegeneration Zebrafish