enkephalin, leucine and Autosomal Dominant Cerebellar Ataxia, Type II

enkephalin, leucine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abe, K; Akechi, Y; Habu, T; Hitomi, T; Ikeda, Y; Kobayashi, H; Koizumi, A; Liu, W; Matsuura, T; Okuda, H	1

Other Studies

1 other study(ies) available for enkephalin, leucine and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement. American journal of human genetics, 2011, Jul-15, Volume: 89, Issue:1 Topics: Adult; Age of Onset; Aged; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Cohort Studies; Enkephalins; Female; Haplotypes; Humans; In Situ Hybridization, Fluorescence; Introns; Lod Score; Male; MicroRNAs; Middle Aged; Motor Neurons; Mutation, Missense; Nuclear Proteins; Pedigree; Protein Precursors; Spinocerebellar Ataxias	2011

Article

Year

Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.

American journal of human genetics, 2011, Jul-15, Volume: 89, Issue:1

Topics: Adult; Age of Onset; Aged; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Cohort Studies; Enkephalins; Female; Haplotypes; Humans; In Situ Hybridization, Fluorescence; Introns; Lod Score; Male; MicroRNAs; Middle Aged; Motor Neurons; Mutation, Missense; Nuclear Proteins; Pedigree; Protein Precursors; Spinocerebellar Ataxias

2011